rs369504169
A SNP in the PROC gene on chromosome 2. Its most notable genotype is A;G: Thrombophilia due to protein C deficiency
- Gene
- PROC
- Location
- Chr 2127,421,337 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadThrombophilia due to protein C deficiency
- G;GGoodcommon in clinvar
On SNPedia: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other PROC SNPs
- rs121918141T;TComplete protein-C deficiency; severe thrombophiliaVery important
- rs121918142C;CComplete protein-C deficiency; severe thrombophiliaVery important
- rs121918143T;TComplete protein-C deficiency; severe thrombophiliaVery important
- rs121918144T;TComplete protein-C deficiency; severe thrombophiliaVery important
- rs121918146A;AComplete protein-C deficiency; severe thrombophiliaVery important
- rs121918147A;AComplete protein-C deficiency; severe thrombophiliaVery important
- rs121918148C;CComplete protein-C deficiency; severe thrombophiliaVery important
- rs121918149A;AComplete protein-C deficiency; severe thrombophiliaVery important
Notes
From SNPedia
Notes
: low anticoagulant activity observed for variant
Source and license
Adapted from rs369504169 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.