rs61756477

A SNP. Its most notable genotype is C;T: Reported to be a pancreatic cancer mutation

Gene
None listed
Highest magnitude
6.0Very important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CGoodcommon/normalTypical · 0.0
  2. C;TMost notableBadReported to be a pancreatic cancer mutationVery important · 6.0

On SNPedia: (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

aka p.Arg184Gln or R184Q Described in a 2019 publication as a mutation in the RABL3 gene pathogenic for pancreatic ductal adenocarcinoma (pancreatic cancer), apparently inherited dominantly.

C;T

see text on main rs-page

Source and license

Adapted from rs61756477 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.