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rs121964948

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Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121964948(A;T)
Make rs121964948(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113147490
GeneF10
is asnp
is mentioned by
dbSNPrs121964948
ebirs121964948
HLIrs121964948
Exacrs121964948
Varsomers121964948
Maprs121964948
PheGenIrs121964948
hapmaprs121964948
1000 genomesrs121964948
hgdprs121964948
ensemblrs121964948
gopubmedrs121964948
geneviewrs121964948
scholarrs121964948
googlers121964948
pharmgkbrs121964948
gwascentralrs121964948
openSNPrs121964948
23andMers121964948
23andMe allrs121964948
SNP Nexus

SNPshotrs121964948
SNPdbers121964948
MSV3drs121964948
GWAS Ctlgrs121964948
Max Magnitude0
OMIM227600
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121964948(T;T)
Alt rs121964948(T;T)
Reference rs121964948(A;A)
Significance Pathogenic
Disease Factor X deficiency
Variation info
Gene F10
CLNDBN Factor X deficiency
Reversed 0
HGVS NC_000013.10:g.113801804A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012839.3,