rs137853096
A SNP in the HSD17B4 gene on chromosome 5. Its most notable genotype is A;A: DBP deficiency (predicted)
- Gene
- HSD17B4
- Location
- Chr 5119,452,621 (GRCh38)
- Highest magnitude
- 7.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadDBP deficiency (predicted)
- A;GBadCarrier of a DBP deficiency mutation
- G;GGoodcommon in clinvar
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
aka c.46G>A (p.Gly16Ser or G16S) 23andMe name: i5007145
A;A
see text and links via main rs-page
A;G
Unaffected in absence of a second HSD17B4 gene mutation
Source and license
Adapted from rs137853096 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.