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rs28933677

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 2.5
(T;T) 3
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904839
GeneF8
is asnp
is mentioned by
dbSNPrs28933677
ebirs28933677
HLIrs28933677
Exacrs28933677
Varsomers28933677
Maprs28933677
PheGenIrs28933677
hapmaprs28933677
1000 genomesrs28933677
hgdprs28933677
ensemblrs28933677
gopubmedrs28933677
geneviewrs28933677
scholarrs28933677
googlers28933677
pharmgkbrs28933677
gwascentralrs28933677
openSNPrs28933677
23andMers28933677
23andMe allrs28933677
SNP Nexus

SNPshotrs28933677
SNPdbers28933677
MSV3drs28933677
GWAS Ctlgrs28933677
Max Magnitude3
OMIM306700
DescHemophilia A
Variant0201
Relatedalso
Neighborrs28933678
Distance321
Neighborrs28933676
Distance25


ClinVar
Risk rs28933677(T;T)
Alt rs28933677(T;T)
Reference rs28933677(C;C)
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.154133114G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010997.3,