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rs121964936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121964936(G;G)
Make rs121964936(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118831
GeneF7
is asnp
is mentioned by
dbSNPrs121964936
ebirs121964936
HLIrs121964936
Exacrs121964936
Varsomers121964936
Maprs121964936
PheGenIrs121964936
hapmaprs121964936
1000 genomesrs121964936
hgdprs121964936
ensemblrs121964936
gopubmedrs121964936
geneviewrs121964936
scholarrs121964936
googlers121964936
pharmgkbrs121964936
gwascentralrs121964936
openSNPrs121964936
23andMers121964936
23andMe allrs121964936
SNP Nexus

SNPshotrs121964936
SNPdbers121964936
MSV3drs121964936
GWAS Ctlgrs121964936
Max Magnitude0
OMIM227500
Desc
Variant0022
Relatedalso
ClinVar
Risk rs121964936(G;G)
Alt rs121964936(G;G)
Reference rs121964936(T;T)
Significance Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113773145T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012869.4,