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rs121964932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121964932(A;G)
Make rs121964932(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113113879
GeneF7
is asnp
is mentioned by
dbSNPrs121964932
ebirs121964932
HLIrs121964932
Exacrs121964932
Varsomers121964932
Maprs121964932
PheGenIrs121964932
hapmaprs121964932
1000 genomesrs121964932
hgdprs121964932
ensemblrs121964932
gopubmedrs121964932
geneviewrs121964932
scholarrs121964932
googlers121964932
pharmgkbrs121964932
gwascentralrs121964932
openSNPrs121964932
23andMers121964932
23andMe allrs121964932
SNP Nexus

SNPshotrs121964932
SNPdbers121964932
MSV3drs121964932
GWAS Ctlgrs121964932
Max Magnitude0
OMIM227500
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121964932(G;G)
Alt rs121964932(G;G)
Reference rs121964932(A;A)
Significance Probable-Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113768193A>G
CLNSRC
CLNACC