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rs387906432

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906432(C;T)
Make rs387906432(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position155022510
GeneF8
is asnp
is mentioned by
dbSNPrs387906432
ebirs387906432
HLIrs387906432
Exacrs387906432
Varsomers387906432
Maprs387906432
PheGenIrs387906432
hapmaprs387906432
1000 genomesrs387906432
hgdprs387906432
ensemblrs387906432
gopubmedrs387906432
geneviewrs387906432
scholarrs387906432
googlers387906432
pharmgkbrs387906432
gwascentralrs387906432
openSNPrs387906432
23andMers387906432
23andMe allrs387906432
SNP Nexus

SNPshotrs387906432
SNPdbers387906432
MSV3drs387906432
GWAS Ctlgrs387906432
Max Magnitude0
ClinVar
Risk rs387906432(T;T)
Alt rs387906432(T;T)
Reference rs387906432(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.154250785G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010865.6,