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rs387906461

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906461(-;-)
Make rs387906461(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154902117
GeneF8
is asnp
is mentioned by
dbSNPrs387906461
ebirs387906461
HLIrs387906461
Exacrs387906461
Varsomers387906461
Maprs387906461
PheGenIrs387906461
hapmaprs387906461
1000 genomesrs387906461
hgdprs387906461
ensemblrs387906461
gopubmedrs387906461
geneviewrs387906461
scholarrs387906461
googlers387906461
pharmgkbrs387906461
gwascentralrs387906461
openSNPrs387906461
23andMers387906461
23andMe allrs387906461
SNP Nexus

SNPshotrs387906461
SNPdbers387906461
MSV3drs387906461
GWAS Ctlgrs387906461
Max Magnitude0
ClinVar
Risk rs387906461(;)
Alt rs387906461(;)
Reference rs387906461(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.154130392delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000011015.4,