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rs121964934

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121964934(G;G)
Make rs121964934(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118772
GeneF7
is asnp
is mentioned by
dbSNPrs121964934
ebirs121964934
HLIrs121964934
Exacrs121964934
Varsomers121964934
Maprs121964934
PheGenIrs121964934
hapmaprs121964934
1000 genomesrs121964934
hgdprs121964934
ensemblrs121964934
gopubmedrs121964934
geneviewrs121964934
scholarrs121964934
googlers121964934
pharmgkbrs121964934
gwascentralrs121964934
openSNPrs121964934
23andMers121964934
23andMe allrs121964934
SNP Nexus

SNPshotrs121964934
SNPdbers121964934
MSV3drs121964934
GWAS Ctlgrs121964934
Max Magnitude0
OMIM227500
Desc
Variant0019
Relatedalso
ClinVar
Risk rs121964934(C,G;C,G)
Alt rs121964934(C,G;C,G)
Reference rs121964934(T;T)
Significance Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113773086T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012866.4,