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

rs28933668

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;C) 0
(C;C) 0 common in clinvar
(C;T) 2.5
(T;T) 3
ReferenceGRCh38 38.1/141
ChromosomeX
Position154966522
GeneF8
is asnp
is mentioned by
dbSNPrs28933668
ebirs28933668
HLIrs28933668
Exacrs28933668
Varsomers28933668
Maprs28933668
PheGenIrs28933668
hapmaprs28933668
1000 genomesrs28933668
hgdprs28933668
ensemblrs28933668
gopubmedrs28933668
geneviewrs28933668
scholarrs28933668
googlers28933668
pharmgkbrs28933668
gwascentralrs28933668
openSNPrs28933668
23andMers28933668
23andMe allrs28933668
SNP Nexus

SNPshotrs28933668
SNPdbers28933668
MSV3drs28933668
GWAS Ctlgrs28933668
Max Magnitude3
OMIM306700
DescHemophilia A
Variant0122
Relatedalso
Neighborrs28933670
Distance39
Neighborrs28933669
Distance1
OMIM306700
Desc
Variant0121
Relatedalso


ClinVar
Risk rs28933668(A,T;A,T)
Alt rs28933668(A,T;A,T)
Reference rs28933668(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.154194797G>A; NC_000023.10:g.154194797G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010918.2, RCV000010917.6,