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rs199469481

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199469481(A;G)
Make rs199469481(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127421420
GenePROC
is asnp
is mentioned by
dbSNPrs199469481
ebirs199469481
HLIrs199469481
Exacrs199469481
Varsomers199469481
Maprs199469481
PheGenIrs199469481
hapmaprs199469481
1000 genomesrs199469481
hgdprs199469481
ensemblrs199469481
gopubmedrs199469481
geneviewrs199469481
scholarrs199469481
googlers199469481
pharmgkbrs199469481
gwascentralrs199469481
openSNPrs199469481
23andMers199469481
23andMe allrs199469481
SNP Nexus

SNPshotrs199469481
SNPdbers199469481
MSV3drs199469481
GWAS Ctlgrs199469481
Max Magnitude0
ClinVar
Risk rs199469481(G;G)
Alt rs199469481(G;G)
Reference rs199469481(A;A)
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.128178996A>G
CLNSRC
CLNACC