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rs387906441

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs387906441(-;-)
Make rs387906441(-;AA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154966499
GeneF8
is asnp
is mentioned by
dbSNPrs387906441
ebirs387906441
HLIrs387906441
Exacrs387906441
Varsomers387906441
Maprs387906441
PheGenIrs387906441
hapmaprs387906441
1000 genomesrs387906441
hgdprs387906441
ensemblrs387906441
gopubmedrs387906441
geneviewrs387906441
scholarrs387906441
googlers387906441
pharmgkbrs387906441
gwascentralrs387906441
openSNPrs387906441
23andMers387906441
23andMe allrs387906441
SNP Nexus

SNPshotrs387906441
SNPdbers387906441
MSV3drs387906441
GWAS Ctlgrs387906441
Max Magnitude0
ClinVar
Risk rs387906441(;)
Alt rs387906441(;)
Reference rs387906441(AA;AA)
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.154194774_154194775delTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000010920.4,