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rs387906458

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906458(-;-)
Make rs387906458(-;T)
Make rs387906458(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904488
GeneF8
is asnp
is mentioned by
dbSNPrs387906458
ebirs387906458
HLIrs387906458
Exacrs387906458
Varsomers387906458
Maprs387906458
PheGenIrs387906458
hapmaprs387906458
1000 genomesrs387906458
hgdprs387906458
ensemblrs387906458
gopubmedrs387906458
geneviewrs387906458
scholarrs387906458
googlers387906458
pharmgkbrs387906458
gwascentralrs387906458
openSNPrs387906458
23andMers387906458
23andMe allrs387906458
SNP Nexus

SNPshotrs387906458
SNPdbers387906458
MSV3drs387906458
GWAS Ctlgrs387906458
Max Magnitude0
ClinVar
Risk rs387906458(T;T)
Alt rs387906458(T;T)
Reference rs387906458(;)
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.154132764dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000011003.5,