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rs121964937

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964937(G;T)
Make rs121964937(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118847
GeneF7
is asnp
is mentioned by
dbSNPrs121964937
ebirs121964937
HLIrs121964937
Exacrs121964937
Varsomers121964937
Maprs121964937
PheGenIrs121964937
hapmaprs121964937
1000 genomesrs121964937
hgdprs121964937
ensemblrs121964937
gopubmedrs121964937
geneviewrs121964937
scholarrs121964937
googlers121964937
pharmgkbrs121964937
gwascentralrs121964937
openSNPrs121964937
23andMers121964937
23andMe allrs121964937
SNP Nexus

SNPshotrs121964937
SNPdbers121964937
MSV3drs121964937
GWAS Ctlgrs121964937
Max Magnitude0
OMIM227500
Desc
Variant0023
Relatedalso
ClinVar
Risk rs121964937(T;T)
Alt rs121964937(T;T)
Reference rs121964937(G;G)
Significance Probable-Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113773161G>T
CLNSRC
CLNACC