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rs369504169

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369504169(A;A)
Make rs369504169(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position127421337
GenePROC
is asnp
is mentioned by
dbSNPrs369504169
ebirs369504169
HLIrs369504169
Exacrs369504169
Varsomers369504169
Maprs369504169
PheGenIrs369504169
hapmaprs369504169
1000 genomesrs369504169
hgdprs369504169
ensemblrs369504169
gopubmedrs369504169
geneviewrs369504169
scholarrs369504169
googlers369504169
pharmgkbrs369504169
gwascentralrs369504169
openSNPrs369504169
23andMers369504169
23andMe allrs369504169
SNP Nexus

SNPshotrs369504169
SNPdbers369504169
MSV3drs369504169
GWAS Ctlgrs369504169
Max Magnitude0
ClinVar
Risk rs369504169(A;A)
Alt rs369504169(A;A)
Reference rs369504169(G;G)
Significance Probable-Pathogenic
Disease Thrombophilia
Variation info
Gene PROC
CLNDBN Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.128178913G>A
CLNSRC ClinVar University of Washington
CLNACC RCV000148739.1,