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rs387906445

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906445(-;-)
Make rs387906445(-;G)
Make rs387906445(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154957112
GeneF8
is asnp
is mentioned by
dbSNPrs387906445
ebirs387906445
HLIrs387906445
Exacrs387906445
Varsomers387906445
Maprs387906445
PheGenIrs387906445
hapmaprs387906445
1000 genomesrs387906445
hgdprs387906445
ensemblrs387906445
gopubmedrs387906445
geneviewrs387906445
scholarrs387906445
googlers387906445
pharmgkbrs387906445
gwascentralrs387906445
openSNPrs387906445
23andMers387906445
23andMe allrs387906445
SNP Nexus

SNPshotrs387906445
SNPdbers387906445
MSV3drs387906445
GWAS Ctlgrs387906445
Max Magnitude0
ClinVar
Risk rs387906445(G;G)
Alt rs387906445(G;G)
Reference rs387906445(;)
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.154185388dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010933.3,