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rs28933669

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 3
(C;T) 2.5
(T;T) 0 common in clinvar
ReferenceGRCh38 38.1/141
ChromosomeX
Position154966523
GeneF8
is asnp
is mentioned by
dbSNPrs28933669
ebirs28933669
HLIrs28933669
Exacrs28933669
Varsomers28933669
Maprs28933669
PheGenIrs28933669
hapmaprs28933669
1000 genomesrs28933669
hgdprs28933669
ensemblrs28933669
gopubmedrs28933669
geneviewrs28933669
scholarrs28933669
googlers28933669
pharmgkbrs28933669
gwascentralrs28933669
openSNPrs28933669
23andMers28933669
23andMe allrs28933669
SNP Nexus

SNPshotrs28933669
SNPdbers28933669
MSV3drs28933669
GWAS Ctlgrs28933669
Max Magnitude3
OMIM306700
DescHemophilia A
Variant0123
Relatedalso
Neighborrs28933668
Distance1
Neighborrs28935499
Distance2


ClinVar
Risk rs28933669(C;C)
Alt rs28933669(C;C)
Reference rs28933669(T;T)
Significance Pathogenic
Disease Hereditary factor VIII deficiency disease
Variation info
Gene F8
CLNDBN Hereditary factor VIII deficiency disease
Reversed 1
HGVS NC_000023.10:g.154194798A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010919.3,