rs281865414
A SNP in the PTPRQ gene on chromosome 12. Its most notable genotype is C;T: Carrier of a recessive mutation for deafness
- Gene
- PTPRQ
- Location
- Chr 1280,460,707 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TGoodcommon in clinvar
- C;TMost notableBadCarrier of a recessive mutation for deafness
SNPedia records rs281865414 on the minus strand: (A;A), (A;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other PTPRQ SNPs
- rs61729287C;TCarrier for a recessive mutation for deafnessImportant
- rs147541734C;TCarrier for a recessive mutation for deafnessImportant
- rs183258549A;GCarrier for a recessive mutation for deafnessImportant
- rs190166486A;GCarrier for a recessive mutation for deafnessImportant
- rs749210663-;ACarrier for a recessive mutation for deafnessImportant
Notes
From SNPedia
Notes
C;T
see PTPRQ gene for details
Source and license
Adapted from rs281865414 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.