Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906451

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906451(-;-)
Make rs387906451(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154930098
GeneF8
is asnp
is mentioned by
dbSNPrs387906451
ebirs387906451
HLIrs387906451
Exacrs387906451
Varsomers387906451
Maprs387906451
PheGenIrs387906451
hapmaprs387906451
1000 genomesrs387906451
hgdprs387906451
ensemblrs387906451
gopubmedrs387906451
geneviewrs387906451
scholarrs387906451
googlers387906451
pharmgkbrs387906451
gwascentralrs387906451
openSNPrs387906451
23andMers387906451
23andMe allrs387906451
SNP Nexus

SNPshotrs387906451
SNPdbers387906451
MSV3drs387906451
GWAS Ctlgrs387906451
Max Magnitude0
ClinVar
Risk rs387906451(;)
Alt rs387906451(;)
Reference rs387906451(C;C)
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.154158373delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000010967.4,