rs121907936
A SNP in the GAA gene on chromosome 17. Its most notable genotype is C;T: Carrier of a GAA gene mutation likely to be pathogenic (for Pompe disease)
- Gene
- GAA
- Location
- Chr 1780,107,894 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;TMost notableBadCarrier of a GAA gene mutation likely to be pathogenic (for Pompe disease)
- T;TGoodcommon in clinvar
On SNPedia: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other GAA SNPs
- rs1800312C;CGlycogen storage disease, type IIVery important
- rs28940868A;Alikely to have Pompe diseaseVery important
- rs121907943T;TGlycogen storage disease II (predicted)Very important
- rs386834236G;GLikely to have Pompe diseaseVery important
- rs28937909A;GCarrier of a glycogen storage disease II mutationImportant
- rs121907939-;AAGCarrier of a glycogen storage disease II mutationImportant
- rs121907945A;GCarrier of a glycogen storage disease II mutationImportant
- rs143523371A;GCarrier of a glycogen storage disease II mutationImportant
Notes
From SNPedia
Notes
aka c.953T>C (p.Met318Thr or M318T), as well as c.953T>A (p.Met318Lys or M318K); the former is annotated in OMIM as pathogenic but as a variant of uncertain significance in ClinVar; the latter is annotated as of uncertain significance in ClinVar.
C;T
see text and links via main rs-page
Source and license
Adapted from rs121907936 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.