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rs28933674

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;G) 0
(A;A) 3
(A;G) 2.5
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904871
GeneF8
is asnp
is mentioned by
dbSNPrs28933674
ebirs28933674
HLIrs28933674
Exacrs28933674
Varsomers28933674
Maprs28933674
PheGenIrs28933674
hapmaprs28933674
1000 genomesrs28933674
hgdprs28933674
ensemblrs28933674
gopubmedrs28933674
geneviewrs28933674
scholarrs28933674
googlers28933674
pharmgkbrs28933674
gwascentralrs28933674
openSNPrs28933674
23andMers28933674
23andMe allrs28933674
SNP Nexus

SNPshotrs28933674
SNPdbers28933674
MSV3drs28933674
GWAS Ctlgrs28933674
Max Magnitude3
OMIM306700
DescHemophilia A
Variant0197
Relatedalso
Neighborrs28933675
Distance4
Neighborrs28935208
Distance2650


ClinVar
Risk rs28933674(A;A)
Alt rs28933674(A;A)
Reference rs28933674(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.154133146C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010993.5,