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rs121918483

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918483(A;A)
Make rs121918483(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position46726734
GeneF2
is asnp
is mentioned by
dbSNPrs121918483
ebirs121918483
HLIrs121918483
Exacrs121918483
Varsomers121918483
Maprs121918483
PheGenIrs121918483
hapmaprs121918483
1000 genomesrs121918483
hgdprs121918483
ensemblrs121918483
gopubmedrs121918483
geneviewrs121918483
scholarrs121918483
googlers121918483
pharmgkbrs121918483
gwascentralrs121918483
openSNPrs121918483
23andMers121918483
23andMe allrs121918483
SNP Nexus

SNPshotrs121918483
SNPdbers121918483
MSV3drs121918483
GWAS Ctlgrs121918483
Max Magnitude0
OMIM176930
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121918483(A;A)
Alt rs121918483(A;A)
Reference rs121918483(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.46748284G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014239.24,