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rs137852459

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852459(A;G)
Make rs137852459(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154896135
GeneF8
is asnp
is mentioned by
dbSNPrs137852459
ebirs137852459
HLIrs137852459
Exacrs137852459
Varsomers137852459
Maprs137852459
PheGenIrs137852459
hapmaprs137852459
1000 genomesrs137852459
hgdprs137852459
ensemblrs137852459
gopubmedrs137852459
geneviewrs137852459
scholarrs137852459
googlers137852459
pharmgkbrs137852459
gwascentralrs137852459
openSNPrs137852459
23andMers137852459
23andMe allrs137852459
SNP Nexus

SNPshotrs137852459
SNPdbers137852459
MSV3drs137852459
GWAS Ctlgrs137852459
Max Magnitude0
OMIM306700
Desc
Variant0227
Relatedalso
ClinVar
Risk rs137852459(G;G)
Alt rs137852459(G;G)
Reference rs137852459(A;A)
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.154124410T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011023.7,