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rs387906446

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906446(C;C)
Make rs387906446(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154956980
GeneF8
is asnp
is mentioned by
dbSNPrs387906446
ebirs387906446
HLIrs387906446
Exacrs387906446
Varsomers387906446
Maprs387906446
PheGenIrs387906446
hapmaprs387906446
1000 genomesrs387906446
hgdprs387906446
ensemblrs387906446
gopubmedrs387906446
geneviewrs387906446
scholarrs387906446
googlers387906446
pharmgkbrs387906446
gwascentralrs387906446
openSNPrs387906446
23andMers387906446
23andMe allrs387906446
SNP Nexus

SNPshotrs387906446
SNPdbers387906446
MSV3drs387906446
GWAS Ctlgrs387906446
Max Magnitude0
ClinVar
Risk rs387906446(C;C)
Alt rs387906446(C;C)
Reference rs387906446(T;T)
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.154185255A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010944.3,