rs121964854
A SNP in the TPM3 gene on chromosome 1. Its most notable genotype is C;C: Nemaline Myopathy 1
- Gene
- TPM3
- Location
- Chr 1154,172,972 (GRCh38)
- Highest magnitude
- 4.0Very important
- Tested on
- Not on consumer chips
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- C;GBadNemaline Myopathy 1
- A;GBadNemaline Myopathy 1
- C;CMost notableBadNemaline Myopathy 1
- A;ABadNemaline Myopathy 1
SNPedia records rs121964854 on the minus strand: (C;C), (C;G), (C;T), (G;G), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Source and license
Adapted from rs121964854 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.