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

rs121964941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121964941(C;C)
Make rs121964941(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113149170
GeneF10
is asnp
is mentioned by
dbSNPrs121964941
ebirs121964941
HLIrs121964941
Exacrs121964941
Varsomers121964941
Maprs121964941
PheGenIrs121964941
hapmaprs121964941
1000 genomesrs121964941
hgdprs121964941
ensemblrs121964941
gopubmedrs121964941
geneviewrs121964941
scholarrs121964941
googlers121964941
pharmgkbrs121964941
gwascentralrs121964941
openSNPrs121964941
23andMers121964941
23andMe allrs121964941
SNP Nexus

SNPshotrs121964941
SNPdbers121964941
MSV3drs121964941
GWAS Ctlgrs121964941
Max Magnitude0
OMIM227600
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121964941(C;C)
Alt rs121964941(C;C)
Reference rs121964941(T;T)
Significance Probable-Pathogenic
Disease Factor X deficiency
Variation info
Gene F10
CLNDBN Factor X deficiency
Reversed 0
HGVS NC_000013.10:g.113803484T>C
CLNSRC
CLNACC