rs1055138

A SNP in the FLJ38576 gene on chromosome 4. Its most notable genotype is G;G: likely to be benign

Gene
FLJ38576
Location
Chr 4186,191,887 (GRCh38)
Highest magnitude
0.5Typical
Tested on
AncestryDNA
Minor allele frequency
44%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodlikely to be benignTypical · 0.514% of people
  2. C;GGoodlikely to be benignTypical · 0.552% of people
  3. C;CGoodcommon in clinvarTypical · 0.033% of people

SNPedia records rs1055138 on the minus strand: (C;C), (C;G), (G;G). 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.

  • Yoruba (Nigeria)G;G 14% C;G 52% C;C 33%

Notes

From SNPedia

Notes

Initially reported in ClinVar as pathogenic, two subsequent reviews have concluded this variant is benign.

G;G

see discussion at rs1055138

C;G

see discussion at rs1055138

Source and license

Adapted from rs1055138 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.