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rs121964927

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964927(G;T)
Make rs121964927(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118716
GeneF7
is asnp
is mentioned by
dbSNPrs121964927
ebirs121964927
HLIrs121964927
Exacrs121964927
Varsomers121964927
Maprs121964927
PheGenIrs121964927
hapmaprs121964927
1000 genomesrs121964927
hgdprs121964927
ensemblrs121964927
gopubmedrs121964927
geneviewrs121964927
scholarrs121964927
googlers121964927
pharmgkbrs121964927
gwascentralrs121964927
openSNPrs121964927
23andMers121964927
23andMe allrs121964927
SNP Nexus

SNPshotrs121964927
SNPdbers121964927
MSV3drs121964927
GWAS Ctlgrs121964927
Max Magnitude0
OMIM227500
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121964927(T;T)
Alt rs121964927(T;T)
Reference rs121964927(G;G)
Significance Probable-Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113773030G>T
CLNSRC
CLNACC