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rs387906440

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs387906440(-;-)
Make rs387906440(-;GA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154966618
GeneF8
is asnp
is mentioned by
dbSNPrs387906440
ebirs387906440
HLIrs387906440
Exacrs387906440
Varsomers387906440
Maprs387906440
PheGenIrs387906440
hapmaprs387906440
1000 genomesrs387906440
hgdprs387906440
ensemblrs387906440
gopubmedrs387906440
geneviewrs387906440
scholarrs387906440
googlers387906440
pharmgkbrs387906440
gwascentralrs387906440
openSNPrs387906440
23andMers387906440
23andMe allrs387906440
SNP Nexus

SNPshotrs387906440
SNPdbers387906440
MSV3drs387906440
GWAS Ctlgrs387906440
Max Magnitude0
ClinVar
Risk rs387906440(;)
Alt rs387906440(;)
Reference rs387906440(GA;GA)
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.154194893_154194894delTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010916.4,