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rs28933681

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 3
(A;G) 2.5
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904401
GeneF8
is asnp
is mentioned by
dbSNPrs28933681
ebirs28933681
HLIrs28933681
Exacrs28933681
Varsomers28933681
Maprs28933681
PheGenIrs28933681
hapmaprs28933681
1000 genomesrs28933681
hgdprs28933681
ensemblrs28933681
gopubmedrs28933681
geneviewrs28933681
scholarrs28933681
googlers28933681
pharmgkbrs28933681
gwascentralrs28933681
openSNPrs28933681
23andMers28933681
23andMe allrs28933681
SNP Nexus

SNPshotrs28933681
SNPdbers28933681
MSV3drs28933681
GWAS Ctlgrs28933681
Max Magnitude3
OMIM306700
DescHemophilia A
Variant0209
Relatedalso
Neighborrs28933682
Distance319
Neighborrs28933680
Distance92


ClinVar
Risk rs28933681(A;A)
Alt rs28933681(A;A)
Reference rs28933681(G;G)
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.154132676C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011005.4,