rs11466532

A SNP in the TGFBR2 gene on chromosome 3. Its most notable genotype is C;C: common in clinvar

Gene
TGFBR2
Location
Chr 330,692,953 (GRCh38)
Highest magnitude
0.0Typical
Tested on
FamilyTreeDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.0100% of people

On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in one HapMap population.

  • European ancestry (Utah)C;C 100%

Other TGFBR2 SNPs

All TGFBR2 SNPs

Source and license

Adapted from rs11466532 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.