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rs121918484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918484(A;A)
Make rs121918484(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position46726761
GeneF2
is asnp
is mentioned by
dbSNPrs121918484
ebirs121918484
HLIrs121918484
Exacrs121918484
Varsomers121918484
Maprs121918484
PheGenIrs121918484
hapmaprs121918484
1000 genomesrs121918484
hgdprs121918484
ensemblrs121918484
gopubmedrs121918484
geneviewrs121918484
scholarrs121918484
googlers121918484
pharmgkbrs121918484
gwascentralrs121918484
openSNPrs121918484
23andMers121918484
23andMe allrs121918484
SNP Nexus

SNPshotrs121918484
SNPdbers121918484
MSV3drs121918484
GWAS Ctlgrs121918484
Max Magnitude0
OMIM176930
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121918484(A;A)
Alt rs121918484(A;A)
Reference rs121918484(G;G)
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.46748311G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014240.25,