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rs199469474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199469474(A;A)
Make rs199469474(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127423397
GenePROC
is asnp
is mentioned by
dbSNPrs199469474
ebirs199469474
HLIrs199469474
Exacrs199469474
Varsomers199469474
Maprs199469474
PheGenIrs199469474
hapmaprs199469474
1000 genomesrs199469474
hgdprs199469474
ensemblrs199469474
gopubmedrs199469474
geneviewrs199469474
scholarrs199469474
googlers199469474
pharmgkbrs199469474
gwascentralrs199469474
openSNPrs199469474
23andMers199469474
23andMe allrs199469474
SNP Nexus

SNPshotrs199469474
SNPdbers199469474
MSV3drs199469474
GWAS Ctlgrs199469474
Max Magnitude0
ClinVar
Risk rs199469474(A;A)
Alt rs199469474(A;A)
Reference rs199469474(G;G)
Significance Probable-Pathogenic
Disease Thrombophilia
Variation info
Gene PROC MIR4783
CLNDBN Thrombophilia, hereditary, due to protein c deficiency, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.128180973G>A
CLNSRC
CLNACC