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rs387906460

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906460(-;-)
Make rs387906460(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154903943
GeneF8
is asnp
is mentioned by
dbSNPrs387906460
ebirs387906460
HLIrs387906460
Exacrs387906460
Varsomers387906460
Maprs387906460
PheGenIrs387906460
hapmaprs387906460
1000 genomesrs387906460
hgdprs387906460
ensemblrs387906460
gopubmedrs387906460
geneviewrs387906460
scholarrs387906460
googlers387906460
pharmgkbrs387906460
gwascentralrs387906460
openSNPrs387906460
23andMers387906460
23andMe allrs387906460
SNP Nexus

SNPshotrs387906460
SNPdbers387906460
MSV3drs387906460
GWAS Ctlgrs387906460
Max Magnitude0
ClinVar
Risk rs387906460(;)
Alt rs387906460(;)
Reference rs387906460(A;A)
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.154132218delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000011014.2,