rs1156044

A SNP in the NDUFV2 gene on chromosome 18. Its most notable genotype is A;A: common in complete genomics

Gene
NDUFV2
Location
Chr 189,102,142 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
22%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in complete genomicsTypical · 0.061% of people

SNPedia records rs1156044 on the minus strand: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageA;A 61%
  • European ancestry (Utah)A;A 69%
  • Han Chinese (Beijing)A;A 49%
  • Japanese (Tokyo)A;A 49%
  • Yoruba (Nigeria)A;A 69%
  • African ancestry (Southwest US)A;A 54%
  • Chinese (Denver)A;A 53%
  • Gujarati IndianA;A 79%
  • Luhya (Kenya)A;A 65%
  • Mexican ancestry (Los Angeles)A;A 62%
  • Maasai (Kenya)A;A 39%
  • TuscanA;A 78%

Conditions, medicines and genes

Other NDUFV2 SNPs

All NDUFV2 SNPs

Notes

From SNPedia

Notes

rs1156044(A) was significantly associated with bipolar disorder (p = 0.013) but differed in allele (rs1156044 G allele) from that previously reported as associated with BD.

Source and license

Adapted from rs1156044 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.