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rs387906430

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906430(C;C)
Make rs387906430(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154969355
GeneF8
is asnp
is mentioned by
dbSNPrs387906430
ebirs387906430
HLIrs387906430
Exacrs387906430
Varsomers387906430
Maprs387906430
PheGenIrs387906430
hapmaprs387906430
1000 genomesrs387906430
hgdprs387906430
ensemblrs387906430
gopubmedrs387906430
geneviewrs387906430
scholarrs387906430
googlers387906430
pharmgkbrs387906430
gwascentralrs387906430
openSNPrs387906430
23andMers387906430
23andMe allrs387906430
SNP Nexus

SNPshotrs387906430
SNPdbers387906430
MSV3drs387906430
GWAS Ctlgrs387906430
Max Magnitude0
ClinVar
Risk rs387906430(C;C)
Alt rs387906430(C;C)
Reference rs387906430(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.154197630A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010854.3,