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rs121964928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964928(A;A)
Make rs121964928(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113117504
GeneF7
is asnp
is mentioned by
dbSNPrs121964928
ebirs121964928
HLIrs121964928
Exacrs121964928
Varsomers121964928
Maprs121964928
PheGenIrs121964928
hapmaprs121964928
1000 genomesrs121964928
hgdprs121964928
ensemblrs121964928
gopubmedrs121964928
geneviewrs121964928
scholarrs121964928
googlers121964928
pharmgkbrs121964928
gwascentralrs121964928
openSNPrs121964928
23andMers121964928
23andMe allrs121964928
SNP Nexus

SNPshotrs121964928
SNPdbers121964928
MSV3drs121964928
GWAS Ctlgrs121964928
Max Magnitude0
OMIM227500
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121964928(A;A)
Alt rs121964928(A;A)
Reference rs121964928(G;G)
Significance Probable-Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113771818G>A
CLNSRC
CLNACC