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rs121964933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121964933(A;A)
Make rs121964933(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position113113893
GeneF7
is asnp
is mentioned by
dbSNPrs121964933
ebirs121964933
HLIrs121964933
Exacrs121964933
Varsomers121964933
Maprs121964933
PheGenIrs121964933
hapmaprs121964933
1000 genomesrs121964933
hgdprs121964933
ensemblrs121964933
gopubmedrs121964933
geneviewrs121964933
scholarrs121964933
googlers121964933
pharmgkbrs121964933
gwascentralrs121964933
openSNPrs121964933
23andMers121964933
23andMe allrs121964933
SNP Nexus

SNPshotrs121964933
SNPdbers121964933
MSV3drs121964933
GWAS Ctlgrs121964933
Max Magnitude0
OMIM227500
Desc
Variant0018
Relatedalso
ClinVar
Risk rs121964933(A;A)
Alt rs121964933(A;A)
Reference rs121964933(C;C)
Significance Probable-Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113768207C>A
CLNSRC
CLNACC