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rs387906437

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906437(-;-)
Make rs387906437(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154969491
GeneF8
is asnp
is mentioned by
dbSNPrs387906437
ebirs387906437
HLIrs387906437
Exacrs387906437
Varsomers387906437
Maprs387906437
PheGenIrs387906437
hapmaprs387906437
1000 genomesrs387906437
hgdprs387906437
ensemblrs387906437
gopubmedrs387906437
geneviewrs387906437
scholarrs387906437
googlers387906437
pharmgkbrs387906437
gwascentralrs387906437
openSNPrs387906437
23andMers387906437
23andMe allrs387906437
SNP Nexus

SNPshotrs387906437
SNPdbers387906437
MSV3drs387906437
GWAS Ctlgrs387906437
Max Magnitude0
ClinVar
Risk rs387906437(;)
Alt rs387906437(;)
Reference rs387906437(T;T)
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.154197766delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000010901.3,