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rs199469475

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs199469475(-;-)
Make rs199469475(-;G)
Make rs199469475(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127427142
GenePROC
is asnp
is mentioned by
dbSNPrs199469475
ebirs199469475
HLIrs199469475
Exacrs199469475
Varsomers199469475
Maprs199469475
PheGenIrs199469475
hapmaprs199469475
1000 genomesrs199469475
hgdprs199469475
ensemblrs199469475
gopubmedrs199469475
geneviewrs199469475
scholarrs199469475
googlers199469475
pharmgkbrs199469475
gwascentralrs199469475
openSNPrs199469475
23andMers199469475
23andMe allrs199469475
SNP Nexus

SNPshotrs199469475
SNPdbers199469475
MSV3drs199469475
GWAS Ctlgrs199469475
Max Magnitude0
ClinVar
Risk rs199469475(G;G)
Alt rs199469475(G;G)
Reference rs199469475(;)
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.128184718dupG
CLNSRC
CLNACC