rs373345919

A SNP in the G6PC gene on chromosome 17. Its most notable genotype is C;T: Carrier of a glycogen storage disease Ia mutation

Gene
G6PC
Location
Chr 1742,909,364 (GRCh38)
Highest magnitude
3.0Important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CGoodcommon/normalTypical · 0.0
  2. C;TMost notableBadCarrier of a glycogen storage disease Ia mutationImportant · 3.0

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

Other G6PC SNPs

All G6PC SNPs

Notes

From SNPedia

Notes

aka c.508C>T (p.Arg170Ter or R170X)

C;T

Unaffected in absence of a second mutation in the G6PC gene

Source and license

Adapted from rs373345919 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.