Have questions? Visit https://www.reddit.com/r/SNPedia

rs121964930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121964930(C;T)
Make rs121964930(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118863
GeneF7
is asnp
is mentioned by
dbSNPrs121964930
ebirs121964930
HLIrs121964930
Exacrs121964930
Varsomers121964930
Maprs121964930
PheGenIrs121964930
hapmaprs121964930
1000 genomesrs121964930
hgdprs121964930
ensemblrs121964930
gopubmedrs121964930
geneviewrs121964930
scholarrs121964930
googlers121964930
pharmgkbrs121964930
gwascentralrs121964930
openSNPrs121964930
23andMers121964930
23andMe allrs121964930
SNP Nexus

SNPshotrs121964930
SNPdbers121964930
MSV3drs121964930
GWAS Ctlgrs121964930
Max Magnitude0
OMIM227500
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121964930(T;T)
Alt rs121964930(T;T)
Reference rs121964930(C;C)
Significance Probable-Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113773177C>T
CLNSRC
CLNACC