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rs121964931

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121964931(C;T)
Make rs121964931(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118518
GeneF7
is asnp
is mentioned by
dbSNPrs121964931
ebirs121964931
HLIrs121964931
Exacrs121964931
Varsomers121964931
Maprs121964931
PheGenIrs121964931
hapmaprs121964931
1000 genomesrs121964931
hgdprs121964931
ensemblrs121964931
gopubmedrs121964931
geneviewrs121964931
scholarrs121964931
googlers121964931
pharmgkbrs121964931
gwascentralrs121964931
openSNPrs121964931
23andMers121964931
23andMe allrs121964931
SNP Nexus

SNPshotrs121964931
SNPdbers121964931
MSV3drs121964931
GWAS Ctlgrs121964931
Max Magnitude0
OMIM227500
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121964931(T;T)
Alt rs121964931(T;T)
Reference rs121964931(C;C)
Significance Probable-Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113772832C>T
CLNSRC
CLNACC