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rs387906429

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906429(A;A)
Make rs387906429(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154991304
GeneF8
is asnp
is mentioned by
dbSNPrs387906429
dbSNP (old)rs387906429
ClinGenrs387906429
ebirs387906429
HLIrs387906429
Exacrs387906429
Gnomadrs387906429
Varsomers387906429
Maprs387906429
PheGenIrs387906429
Biobankrs387906429
1000 genomesrs387906429
hgdprs387906429
ensemblrs387906429
gopubmedrs387906429
geneviewrs387906429
scholarrs387906429
googlers387906429
pharmgkbrs387906429
gwascentralrs387906429
openSNPrs387906429
23andMers387906429
23andMe allrs387906429
SNP Nexus

SNPshotrs387906429
SNPdbers387906429
MSV3drs387906429
GWAS Ctlgrs387906429
Max Magnitude0
ClinVar
Risk rs387906429(A;A)
Alt rs387906429(A;A)
Reference Rs387906429(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.154219579C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010809.2,