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rs199469482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199469482(A;A)
Make rs199469482(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127421454
GenePROC
is asnp
is mentioned by
dbSNPrs199469482
ebirs199469482
HLIrs199469482
Exacrs199469482
Varsomers199469482
Maprs199469482
PheGenIrs199469482
hapmaprs199469482
1000 genomesrs199469482
hgdprs199469482
ensemblrs199469482
gopubmedrs199469482
geneviewrs199469482
scholarrs199469482
googlers199469482
pharmgkbrs199469482
gwascentralrs199469482
openSNPrs199469482
23andMers199469482
23andMe allrs199469482
SNP Nexus

SNPshotrs199469482
SNPdbers199469482
MSV3drs199469482
GWAS Ctlgrs199469482
Max Magnitude0
ClinVar
Risk rs199469482(A;A)
Alt rs199469482(A;A)
Reference rs199469482(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.128179030G>A
CLNSRC
CLNACC