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rs121918486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918486(C;G)
Make rs121918486(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position46739324
GeneF2
is asnp
is mentioned by
dbSNPrs121918486
ebirs121918486
HLIrs121918486
Exacrs121918486
Varsomers121918486
Maprs121918486
PheGenIrs121918486
hapmaprs121918486
1000 genomesrs121918486
hgdprs121918486
ensemblrs121918486
gopubmedrs121918486
geneviewrs121918486
scholarrs121918486
googlers121918486
pharmgkbrs121918486
gwascentralrs121918486
openSNPrs121918486
23andMers121918486
23andMe allrs121918486
SNP Nexus

SNPshotrs121918486
SNPdbers121918486
MSV3drs121918486
GWAS Ctlgrs121918486
Max Magnitude0
OMIM176930
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121918486(G;G)
Alt rs121918486(G;G)
Reference rs121918486(C;C)
Significance Pathogenic
Disease Hereditary factor II deficiency disease
Variation info
Gene F2
CLNDBN Hereditary factor II deficiency disease
Reversed 0
HGVS NC_000011.9:g.46760874C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014242.17,