rs2001030
A SNP on chromosome MT. Its most notable genotype is A;A: common in clinvar
- Gene
- None listed
- Location
- Chr MT1,438 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 4%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageA;A 7% G;G 93%
- European ancestry (Utah)A;A 5% G;G 95%
- Han Chinese (Beijing)A;A 5% G;G 96%
- Japanese (Tokyo)A;A 0% G;G 100%
- Yoruba (Nigeria)A;A 19% G;G 81%
Related
Genosets
- Gs1018Mitochondrial Haplogroup H2a1Worth knowing
- Gs1019Mitochondrial Haplogroup H2a2Worth knowing
- Gs1017Mitochondrial Haplogroup H2aWorth knowing
- Gs1016Mitochondrial Haplogroup H2Minor
- Gs1025Mitochondrial Haplogroup H2a5Minor
- Gs1015Mitochondrial Haplogroup H18Minor
- Gs1022Mitochondrial Haplogroup H2a2b1Minor
- Gs1023Mitochondrial Haplogroup H2a3Minor
- Gs1024Mitochondrial Haplogroup H2a4Minor
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Notes
haplogroups
Source and license
Adapted from rs2001030 on 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.