rs5030814(G;G)

If from 23andMe, normal genotype

Magnitude
0.0Typical
Repute
Good
On SNPedia
rs5030814(G;G)
Gene
VHL

Other genotypes of rs5030814

  1. G;TMost notableBadVon Hippel-Lindau syndrome mutationVery important · 7.0
  2. T;TGoodcommon in clinvarTypical · 0.0

All about rs5030814

Notes

From SNPedia

If viewed in a Promethease report, and from 23andMe data, this represents an error by 23andMe, in that they associate rs5030814 with chromosomal position GRCh37 3:10188321, whereas it is actually designated in the NIH dbSNP database as being at position 3:10188322. At position 3:10188321, the normal genotype on the plus/fwd strand is (G;G). That is not the normal genotype for rs5030814, however, if it is properly annotated. If your data is not from 23andMe, feel free to contact us to discuss this.

Source and license

Adapted from rs5030814(G;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.