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rs387906464

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906464(-;-)
Make rs387906464(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154861742
GeneF8
is asnp
is mentioned by
dbSNPrs387906464
ebirs387906464
HLIrs387906464
Exacrs387906464
Varsomers387906464
Maprs387906464
PheGenIrs387906464
hapmaprs387906464
1000 genomesrs387906464
hgdprs387906464
ensemblrs387906464
gopubmedrs387906464
geneviewrs387906464
scholarrs387906464
googlers387906464
pharmgkbrs387906464
gwascentralrs387906464
openSNPrs387906464
23andMers387906464
23andMe allrs387906464
SNP Nexus

SNPshotrs387906464
SNPdbers387906464
MSV3drs387906464
GWAS Ctlgrs387906464
Max Magnitude0
ClinVar
Risk rs387906464(;)
Alt rs387906464(;)
Reference rs387906464(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.154090017delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000011039.3,