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rs121964947

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964947(A;A)
Make rs121964947(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113149062
GeneF10
is asnp
is mentioned by
dbSNPrs121964947
ebirs121964947
HLIrs121964947
Exacrs121964947
Varsomers121964947
Maprs121964947
PheGenIrs121964947
hapmaprs121964947
1000 genomesrs121964947
hgdprs121964947
ensemblrs121964947
gopubmedrs121964947
geneviewrs121964947
scholarrs121964947
googlers121964947
pharmgkbrs121964947
gwascentralrs121964947
openSNPrs121964947
23andMers121964947
23andMe allrs121964947
SNP Nexus

SNPshotrs121964947
SNPdbers121964947
MSV3drs121964947
GWAS Ctlgrs121964947
Max Magnitude0
OMIM227600
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121964947(A;A)
Alt rs121964947(A;A)
Reference rs121964947(G;G)
Significance Probable-Pathogenic
Disease Factor X deficiency
Variation info
Gene F10
CLNDBN Factor X deficiency
Reversed 0
HGVS NC_000013.10:g.113803376G>A
CLNSRC
CLNACC