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rs387906438

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906438(-;-)
Make rs387906438(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154969433
GeneF8
is asnp
is mentioned by
dbSNPrs387906438
ebirs387906438
HLIrs387906438
Exacrs387906438
Varsomers387906438
Maprs387906438
PheGenIrs387906438
hapmaprs387906438
1000 genomesrs387906438
hgdprs387906438
ensemblrs387906438
gopubmedrs387906438
geneviewrs387906438
scholarrs387906438
googlers387906438
pharmgkbrs387906438
gwascentralrs387906438
openSNPrs387906438
23andMers387906438
23andMe allrs387906438
SNP Nexus

SNPshotrs387906438
SNPdbers387906438
MSV3drs387906438
GWAS Ctlgrs387906438
Max Magnitude0
ClinVar
Risk rs387906438(;)
Alt rs387906438(;)
Reference rs387906438(G;G)
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.154197708delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010907.5,