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rs387906455

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906455(-;-)
Make rs387906455(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154929411
GeneF8
is asnp
is mentioned by
dbSNPrs387906455
ebirs387906455
HLIrs387906455
Exacrs387906455
Varsomers387906455
Maprs387906455
PheGenIrs387906455
hapmaprs387906455
1000 genomesrs387906455
hgdprs387906455
ensemblrs387906455
gopubmedrs387906455
geneviewrs387906455
scholarrs387906455
googlers387906455
pharmgkbrs387906455
gwascentralrs387906455
openSNPrs387906455
23andMers387906455
23andMe allrs387906455
SNP Nexus

SNPshotrs387906455
SNPdbers387906455
MSV3drs387906455
GWAS Ctlgrs387906455
Max Magnitude0
ClinVar
Risk rs387906455(;)
Alt rs387906455(;)
Reference rs387906455(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.154157686delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000010974.6,