Mitochondrial DNA
80 well-documented SNPs on mitochondrial dna, in order of position (GRCh38).
- rs3937039663T;TNo summary available.Typical
- rs56489998663T;Tcommon in complete genomicsTypical
- rs20009741,048C;Ccommon on affy axiom dataTypical
- rs283585721,243T;Tcommon on affy axiom dataTypical
- rs20010301,438A;Acommon in clinvarTypical
- rs2676066171,555G;GHigh risk of developing hearing loss after taking aminoglycoside antibioticsVery important
- rs39283051,719A;GHeteroplasmyImportant
- rs283585741,738A;ANo summary available.Typical
- rs283585761,811A;ANo summary available.Typical
- rs283585771,888G;Gcommon on affy axiom dataTypical
- rs28541282,706A;AG2706A+, probably MT-Haplogroup H.Minor
- rs28541302,885T;Tcommon on affy axiom dataTypical
- rs39283063,010G;Gcommon on affy axiom dataTypical
- rs28358582ND1 · 3,308T;Tcommon in clinvarTypical
- rs28358584ND1 · 3,480A;ANo summary available.Typical
- rs2854134ND1 · 3,593C;Ccommon genotypeTypical
- rs28357968ND1 · 3,666G;GNo summary available.Typical
- rs28357970ND1 · 3,796A;Acommon in clinvarTypical
- rs1599988ND1 · 4,216T;Tcommon in clinvarTypical
- rs28357976ND2 · 4,715A;Acommon in complete genomicsTypical
- rs3021086ND2 · 4,769A;GNo summary available.Typical
- rs28357980ND2 · 4,917A;AnormalTypical
- rs3020601ND2 · 5,442T;TNo summary available.Typical
- rs3021088ND2 · 5,460A;ANo summary available.Typical
- rs96592395,773G;Gcommon in complete genomicsTypical
- rs1029272COX1 · 6,185T;TNo summary available.Typical
- rs2015062COX1 · 7,028T;Tcommon on affy axiom dataTypical
- rs28358875COX1 · 7,196C;Ccommon in complete genomicsTypical
- rs3021089COX2 · 8,251G;GNo summary available.Typical
- rs1116907ATP8 · 8,468C;Ccommon genotypeTypical
- rs2298007ATP6 · 8,794C;Ccommon in complete genomicsTypical
- rs28358887ATP6 · 8,994G;GNo summary available.Typical
- rs3020605ATP6 · 9,042C;CNo summary available.Typical
- rs386829069ATP6 · 9,191C;CLikely miscall if from Ancestry data; otherwise, Leigh syndrome mutationImportant
- rs2853824COX3 · 9,347T;TNo summary available.Typical
- rs9743COX3 · 9,698T;TNo summary available.Typical
- rs2853826ND3 · 10,398A;Acommon in clinvarTypical
- rs28358278ND3 · 10,400C;Ccommon genotypeTypical
- rs2835827910,463T;TNo summary available.Typical
- rs28358280ND4L · 10,550A;ANo summary available.Typical
- rs2853487ND4L · 10,589G;GNo summary available.Typical
- rs2854121MT-ND4L · 10,663C;CNo summary available.Typical
- rs2853488ND4L · 10,688G;Gcommon genotypeTypical
- rs2857284ND4 · 10,873C;CNo summary available.Typical
- rs2857285ND4 · 10,915T;TNo summary available.Typical
- rs3915952MT-ND4 · 11,251A;ANo summary available.Typical
- rs28358285ND4 · 11,299T;TNo summary available.Typical
- rs2853493ND4 · 11,467G;GA11467G+, MT-Haplogroup U or KMinor
- rs28358286ND4 · 11,674C;CNo summary available.Typical
- i5000099MT-ND4 · 11,778A;AMELAS syndromeVery important
- rs199476112ND4 · 11,778A;ALeber's Optic AtrophyVery important
- rs2853496ND4 · 11,914G;Gcommon genotypeTypical
- rs28359168ND4 · 11,947A;ANo summary available.Typical
- rs2853497ND4 · 12,007G;GNo summary available.Typical
- rs285349812,308G;G12308+, MT-Haplogroup U or K.Minor
- rs2853499ND5 · 12,372A;AG12372A+, MT-Haplogroup U or KMinor
- rs28359172ND5 · 12,612A;ANo summary available.Typical
- rs2853500ND5 · 12,720A;ANo summary available.Typical
- rs2853501ND5 · 13,105A;Acommon genotypeTypical
- rs28359175ND5 · 13,263A;ANo summary available.Typical
- rs2853502ND5 · 13,276A;ANo summary available.Typical
- rs3899498ND5 · 13,368G;GNo summary available.Typical
- rs2857287ND5 · 13,506C;Ccommon genotypeTypical
- rs28359178ND5 · 13,708G;GNo summary available.Typical
- rs28359179ND5 · 13,789T;TNo summary available.Typical
- rs28359184ND5 · 13,928G;GNo summary available.Typical
- rs28357670MT-CYB · 14,167C;CNo summary available.Typical
- rs28357671ND6 · 14,178T;TNo summary available.Typical
- rs28357675ND6 · 14,318T;TNo summary available.Typical
- rs199476104ND6 · 14,484C;CLeber's Optic AtrophyVery important
- rs28357676ND6 · 14,560G;GNo summary available.Typical
- rs28357681CYTB · 14,798T;Tcommon on affy axiom dataTypical
- rs28357369CYTB · 15,244A;ANo summary available.Typical
- rs527236045CYTB · 15,301G;Gcommon in clinvarTypical
- rs2853508CYTB · 15,326A;Acommon in clinvarTypical
- rs3088309MT-CYB · 15,452C;CNo summary available.Typical
- rs527236209CYTB · 15,452C;Ccommon in clinvarTypical
- rs28357372MT-CYB · 15,607A;ANo summary available.Typical
- rs527236210CYTB · 15,607A;Acommon in clinvarTypical
- rs285412516,147C;CNo summary available.Typical
No matches.
Source and license
Adapted from SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.