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rs28937294

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28937294(A;A)
Make rs28937294(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904025
GeneF8
is asnp
is mentioned by
dbSNPrs28937294
ebirs28937294
HLIrs28937294
Exacrs28937294
Varsomers28937294
Maprs28937294
PheGenIrs28937294
hapmaprs28937294
1000 genomesrs28937294
hgdprs28937294
ensemblrs28937294
gopubmedrs28937294
geneviewrs28937294
scholarrs28937294
googlers28937294
pharmgkbrs28937294
gwascentralrs28937294
openSNPrs28937294
23andMers28937294
23andMe allrs28937294
SNP Nexus

SNPshotrs28937294
SNPdbers28937294
MSV3drs28937294
GWAS Ctlgrs28937294
Max Magnitude0
OMIM306700
DescHemophilia A
Variant0026
Relatedalso
Neighborrs28937295
Distance21
Neighborrs28933682
Distance57
OMIM306700
Desc
Variant0212
Relatedalso
ClinVar
Risk rs28937294(A,T;A,T)
Alt rs28937294(A,T;A,T)
Reference rs28937294(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.154132300C>A; NC_000023.10:g.154132300C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011008.4, RCV000010822.2,