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rs397514036

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397514036(-;-)
Make rs397514036(-;A)
Make rs397514036(A;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154928964
GeneF8
is asnp
is mentioned by
dbSNPrs397514036
ebirs397514036
HLIrs397514036
Exacrs397514036
Varsomers397514036
Maprs397514036
PheGenIrs397514036
hapmaprs397514036
1000 genomesrs397514036
hgdprs397514036
ensemblrs397514036
gopubmedrs397514036
geneviewrs397514036
scholarrs397514036
googlers397514036
pharmgkbrs397514036
gwascentralrs397514036
openSNPrs397514036
23andMers397514036
23andMe allrs397514036
SNP Nexus

SNPshotrs397514036
SNPdbers397514036
MSV3drs397514036
GWAS Ctlgrs397514036
Max Magnitude0
ClinVar
Risk rs397514036(A;A)
Alt rs397514036(A;A)
Reference rs397514036(;)
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.154157240dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000010976.4,