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rs387906454

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
Make rs387906454(-;-)
Make rs387906454(-;AAGA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154929459
GeneF8
is asnp
is mentioned by
dbSNPrs387906454
ebirs387906454
HLIrs387906454
Exacrs387906454
Varsomers387906454
Maprs387906454
PheGenIrs387906454
hapmaprs387906454
1000 genomesrs387906454
hgdprs387906454
ensemblrs387906454
gopubmedrs387906454
geneviewrs387906454
scholarrs387906454
googlers387906454
pharmgkbrs387906454
gwascentralrs387906454
openSNPrs387906454
23andMers387906454
23andMe allrs387906454
SNP Nexus

SNPshotrs387906454
SNPdbers387906454
MSV3drs387906454
GWAS Ctlgrs387906454
Max Magnitude0
ClinVar
Risk rs387906454(;)
Alt rs387906454(;)
Reference rs387906454(AAGA;AAGA)
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.154157734_154157737delTCTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000010972.5,