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rs121918485

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918485(A;A)
Make rs121918485(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position46728139
GeneF2
is asnp
is mentioned by
dbSNPrs121918485
ebirs121918485
HLIrs121918485
Exacrs121918485
Varsomers121918485
Maprs121918485
PheGenIrs121918485
hapmaprs121918485
1000 genomesrs121918485
hgdprs121918485
ensemblrs121918485
gopubmedrs121918485
geneviewrs121918485
scholarrs121918485
googlers121918485
pharmgkbrs121918485
gwascentralrs121918485
openSNPrs121918485
23andMers121918485
23andMe allrs121918485
SNP Nexus

SNPshotrs121918485
SNPdbers121918485
MSV3drs121918485
GWAS Ctlgrs121918485
Max Magnitude0
OMIM176930
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121918485(A;A)
Alt rs121918485(A;A)
Reference rs121918485(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.46749689G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014241.23,