rs104894128

A SNP in the TPM2 gene on chromosome 9. Its most notable genotype is G;G: Nemaline Myopathy 4

Gene
TPM2
Location
Chr 935,685,486 (GRCh38)
Highest magnitude
4.0Very important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TGoodcommon in clinvarTypical · 0.0
  2. G;TBadNemaline Myopathy 4Worth knowing · 2.0
  3. G;GMost notableBadNemaline Myopathy 4Very important · 4.0

SNPedia records rs104894128 on the minus strand: (A;A), (A;C), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other TPM2 SNPs

All TPM2 SNPs

Source and license

Adapted from rs104894128 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.