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rs121964935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964935(A;A)
Make rs121964935(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113110812
GeneF7
is asnp
is mentioned by
dbSNPrs121964935
ebirs121964935
HLIrs121964935
Exacrs121964935
Varsomers121964935
Maprs121964935
PheGenIrs121964935
hapmaprs121964935
1000 genomesrs121964935
hgdprs121964935
ensemblrs121964935
gopubmedrs121964935
geneviewrs121964935
scholarrs121964935
googlers121964935
pharmgkbrs121964935
gwascentralrs121964935
openSNPrs121964935
23andMers121964935
23andMe allrs121964935
SNP Nexus

SNPshotrs121964935
SNPdbers121964935
MSV3drs121964935
GWAS Ctlgrs121964935
Max Magnitude0
OMIM227500
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121964935(A;A)
Alt rs121964935(A;A)
Reference rs121964935(G;G)
Significance Probable-Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113765126G>A
CLNSRC
CLNACC