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rs199469476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199469476(A;A)
Make rs199469476(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127426181
GenePROC
is asnp
is mentioned by
dbSNPrs199469476
ebirs199469476
HLIrs199469476
Exacrs199469476
Varsomers199469476
Maprs199469476
PheGenIrs199469476
hapmaprs199469476
1000 genomesrs199469476
hgdprs199469476
ensemblrs199469476
gopubmedrs199469476
geneviewrs199469476
scholarrs199469476
googlers199469476
pharmgkbrs199469476
gwascentralrs199469476
openSNPrs199469476
23andMers199469476
23andMe allrs199469476
SNP Nexus

SNPshotrs199469476
SNPdbers199469476
MSV3drs199469476
GWAS Ctlgrs199469476
Merged fromRs28933987
Max Magnitude0
ClinVar
Risk rs199469476(A;A)
Alt rs199469476(A;A)
Reference rs199469476(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.128183757G>A
CLNSRC
CLNACC