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rs118203911

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs118203911(C;C)
Make rs118203911(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169552693
GeneF5
is asnp
is mentioned by
dbSNPrs118203911
ebirs118203911
HLIrs118203911
Exacrs118203911
Varsomers118203911
Maprs118203911
PheGenIrs118203911
hapmaprs118203911
1000 genomesrs118203911
hgdprs118203911
ensemblrs118203911
gopubmedrs118203911
geneviewrs118203911
scholarrs118203911
googlers118203911
pharmgkbrs118203911
gwascentralrs118203911
openSNPrs118203911
23andMers118203911
23andMe allrs118203911
SNP Nexus

SNPshotrs118203911
SNPdbers118203911
MSV3drs118203911
GWAS Ctlgrs118203911
Max Magnitude0
OMIM612309
Desc
Variant0013
Relatedalso
ClinVar
Risk rs118203911(C;C)
Alt rs118203911(C;C)
Reference rs118203911(T;T)
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.169521931A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000689.2,