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rs387906457

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906457(A;T)
Make rs387906457(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904918
GeneF8
is asnp
is mentioned by
dbSNPrs387906457
ebirs387906457
HLIrs387906457
Exacrs387906457
Varsomers387906457
Maprs387906457
PheGenIrs387906457
hapmaprs387906457
1000 genomesrs387906457
hgdprs387906457
ensemblrs387906457
gopubmedrs387906457
geneviewrs387906457
scholarrs387906457
googlers387906457
pharmgkbrs387906457
gwascentralrs387906457
openSNPrs387906457
23andMers387906457
23andMe allrs387906457
SNP Nexus

SNPshotrs387906457
SNPdbers387906457
MSV3drs387906457
GWAS Ctlgrs387906457
Max Magnitude0
ClinVar
Risk rs387906457(T;T)
Alt rs387906457(T;T)
Reference rs387906457(A;A)
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.154133193T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010996.4,