rs1064793762

A SNP in the MIR6511B1 gene on chromosome 16. Its most notable genotype is A;G: Polycystic Kidney Disease likely, but see discussion

Gene
MIR6511B1
Location
Chr 162,108,254 (GRCh38)
Highest magnitude
5.0Very important
Tested on
Not on consumer chips

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GGoodcommon in clinvarTypical · 0.0
  2. A;GMost notableBadPolycystic Kidney Disease likely, but see discussionVery important · 5.0

SNPedia records rs1064793762 on the minus strand: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Notes

From SNPedia

Notes

c.6913C>T (p.Gln2305Ter) It's likely that the variant allele is pathogenic for autosomal dominant polycystic kidney disease, given the way it is listed in ClinVar, however, it's also possible that it's associated with (only) the recessive form; the ClinVar submitter, GeneDX, did not provide additional details. If any expert has evidence indicating which it is associated with (dominant or recessive) please contact us or leave details on the Discussion page for this SNP.

A;G

See discussion on main rs-page about recessive vs dominant inheritance.

Source and license

Adapted from rs1064793762 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.