Have questions? Visit https://www.reddit.com/r/SNPedia

rs118203912

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203912(G;T)
Make rs118203912(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169560701
GeneF5
is asnp
is mentioned by
dbSNPrs118203912
ebirs118203912
HLIrs118203912
Exacrs118203912
Varsomers118203912
Maprs118203912
PheGenIrs118203912
hapmaprs118203912
1000 genomesrs118203912
hgdprs118203912
ensemblrs118203912
gopubmedrs118203912
geneviewrs118203912
scholarrs118203912
googlers118203912
pharmgkbrs118203912
gwascentralrs118203912
openSNPrs118203912
23andMers118203912
23andMe allrs118203912
SNP Nexus

SNPshotrs118203912
SNPdbers118203912
MSV3drs118203912
GWAS Ctlgrs118203912
Max Magnitude0
OMIM612309
Desc
Variant0014
Relatedalso
ClinVar
Risk rs118203912(T;T)
Alt rs118203912(T;T)
Reference rs118203912(G;G)
Significance Pathogenic
Disease Thrombophilia due to activated protein C resistance
Variation info
Gene F5
CLNDBN Thrombophilia due to activated protein C resistance
Reversed 1
HGVS NC_000001.10:g.169529939C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000679.2,