i5006200

A SNP in the BSCL2 gene on chromosome 11. Its most notable genotype is G;G: Congenital generalized lipodystrophy, type 2

Gene
BSCL2
Location
Chr 1162,459,885 (GRCh38)
Highest magnitude
6.0Very important
Tested on
23andMe

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CGoodcommon/normalTypical · 0.0
  2. C;GBadcarrier of one congenital generalized lipodystrophy alleleImportant · 3.0
  3. G;GMost notableBadCongenital generalized lipodystrophy, type 2Very important · 6.0

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

Notes

From SNPedia

Notes

rs137852971 congenital generalized lipodystrophy

C;G

see discussion at rs137852971

G;G

see discussion at rs137852971

Source and license

Adapted from i5006200 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.