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rs387906442

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906442(-;-)
Make rs387906442(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154966120
GeneF8
is asnp
is mentioned by
dbSNPrs387906442
ebirs387906442
HLIrs387906442
Exacrs387906442
Varsomers387906442
Maprs387906442
PheGenIrs387906442
hapmaprs387906442
1000 genomesrs387906442
hgdprs387906442
ensemblrs387906442
gopubmedrs387906442
geneviewrs387906442
scholarrs387906442
googlers387906442
pharmgkbrs387906442
gwascentralrs387906442
openSNPrs387906442
23andMers387906442
23andMe allrs387906442
SNP Nexus

SNPshotrs387906442
SNPdbers387906442
MSV3drs387906442
GWAS Ctlgrs387906442
Max Magnitude0
ClinVar
Risk rs387906442(;)
Alt rs387906442(;)
Reference rs387906442(G;G)
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.154194395delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010924.2,