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rs387906439

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906439(-;-)
Make rs387906439(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154969397
GeneF8
is asnp
is mentioned by
dbSNPrs387906439
ebirs387906439
HLIrs387906439
Exacrs387906439
Varsomers387906439
Maprs387906439
PheGenIrs387906439
hapmaprs387906439
1000 genomesrs387906439
hgdprs387906439
ensemblrs387906439
gopubmedrs387906439
geneviewrs387906439
scholarrs387906439
googlers387906439
pharmgkbrs387906439
gwascentralrs387906439
openSNPrs387906439
23andMers387906439
23andMe allrs387906439
SNP Nexus

SNPshotrs387906439
SNPdbers387906439
MSV3drs387906439
GWAS Ctlgrs387906439
Max Magnitude0
ClinVar
Risk rs387906439(;)
Alt rs387906439(;)
Reference rs387906439(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.154197672delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010911.7,