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rs121964926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964926(A;A)
Make rs121964926(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118698
GeneF7
is asnp
is mentioned by
dbSNPrs121964926
ebirs121964926
HLIrs121964926
Exacrs121964926
Varsomers121964926
Maprs121964926
PheGenIrs121964926
hapmaprs121964926
1000 genomesrs121964926
hgdprs121964926
ensemblrs121964926
gopubmedrs121964926
geneviewrs121964926
scholarrs121964926
googlers121964926
pharmgkbrs121964926
gwascentralrs121964926
openSNPrs121964926
23andMers121964926
23andMe allrs121964926
SNP Nexus

SNPshotrs121964926
SNPdbers121964926
MSV3drs121964926
GWAS Ctlgrs121964926
GMAF0.003673
Max Magnitude0
OMIM227500
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121964926(A;A)
Alt rs121964926(A;A)
Reference rs121964926(G;G)
Significance Probable-Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113773012G>A
CLNSRC
CLNACC