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

rs118203906

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203906(C;C)
Make rs118203906(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169555299
GeneF5
is asnp
is mentioned by
dbSNPrs118203906
ebirs118203906
HLIrs118203906
Exacrs118203906
Varsomers118203906
Maprs118203906
PheGenIrs118203906
hapmaprs118203906
1000 genomesrs118203906
hgdprs118203906
ensemblrs118203906
gopubmedrs118203906
geneviewrs118203906
scholarrs118203906
googlers118203906
pharmgkbrs118203906
gwascentralrs118203906
openSNPrs118203906
23andMers118203906
23andMe allrs118203906
SNP Nexus

SNPshotrs118203906
SNPdbers118203906
MSV3drs118203906
GWAS Ctlgrs118203906
GMAF0.0004591
Max Magnitude0
OMIM612309
Desc
Variant0003
Relatedalso
ClinVar
Risk rs118203906(C;C)
Alt rs118203906(C;C)
Reference rs118203906(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.169524537C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000678.2,