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rs199469470

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199469470(G;G)
Make rs199469470(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127426090
GenePROC
is asnp
is mentioned by
dbSNPrs199469470
ebirs199469470
HLIrs199469470
Exacrs199469470
Varsomers199469470
Maprs199469470
PheGenIrs199469470
hapmaprs199469470
1000 genomesrs199469470
hgdprs199469470
ensemblrs199469470
gopubmedrs199469470
geneviewrs199469470
scholarrs199469470
googlers199469470
pharmgkbrs199469470
gwascentralrs199469470
openSNPrs199469470
23andMers199469470
23andMe allrs199469470
SNP Nexus

SNPshotrs199469470
SNPdbers199469470
MSV3drs199469470
GWAS Ctlgrs199469470
Max Magnitude0
ClinVar
Risk rs199469470(G;G)
Alt rs199469470(G;G)
Reference rs199469470(T;T)
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.128183666T>G
CLNSRC
CLNACC