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rs387906435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs387906435(-;-)
Make rs387906435(-;GT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154996996
GeneF8
is asnp
is mentioned by
dbSNPrs387906435
ebirs387906435
HLIrs387906435
Exacrs387906435
Varsomers387906435
Maprs387906435
PheGenIrs387906435
hapmaprs387906435
1000 genomesrs387906435
hgdprs387906435
ensemblrs387906435
gopubmedrs387906435
geneviewrs387906435
scholarrs387906435
googlers387906435
pharmgkbrs387906435
gwascentralrs387906435
openSNPrs387906435
23andMers387906435
23andMe allrs387906435
SNP Nexus

SNPshotrs387906435
SNPdbers387906435
MSV3drs387906435
GWAS Ctlgrs387906435
Max Magnitude0
ClinVar
Risk rs387906435(;)
Alt rs387906435(;)
Reference rs387906435(GT;GT)
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.154225271_154225272delAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010873.6,