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rs142742242

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142742242(A;A)
Make rs142742242(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position127428761
GenePROC
is asnp
is mentioned by
dbSNPrs142742242
ebirs142742242
HLIrs142742242
Exacrs142742242
Varsomers142742242
Maprs142742242
PheGenIrs142742242
hapmaprs142742242
1000 genomesrs142742242
hgdprs142742242
ensemblrs142742242
gopubmedrs142742242
geneviewrs142742242
scholarrs142742242
googlers142742242
pharmgkbrs142742242
gwascentralrs142742242
openSNPrs142742242
23andMers142742242
23andMe allrs142742242
SNP Nexus

SNPshotrs142742242
SNPdbers142742242
MSV3drs142742242
GWAS Ctlgrs142742242
Max Magnitude0
ClinVar
Risk rs142742242(A;A)
Alt rs142742242(A;A)
Reference rs142742242(G;G)
Significance Pathogenic
Disease Thrombophilia
Variation info
Gene PROC
CLNDBN Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.128186337G>A
CLNSRC ClinVar University of Washington
CLNACC RCV000148740.1,