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rs137852362

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852362(A;G)
Make rs137852362(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154928607
GeneF8
is asnp
is mentioned by
dbSNPrs137852362
ebirs137852362
HLIrs137852362
Exacrs137852362
Varsomers137852362
Maprs137852362
PheGenIrs137852362
hapmaprs137852362
1000 genomesrs137852362
hgdprs137852362
ensemblrs137852362
gopubmedrs137852362
geneviewrs137852362
scholarrs137852362
googlers137852362
pharmgkbrs137852362
gwascentralrs137852362
openSNPrs137852362
23andMers137852362
23andMe allrs137852362
SNP Nexus

SNPshotrs137852362
SNPdbers137852362
MSV3drs137852362
GWAS Ctlgrs137852362
Max Magnitude0
OMIM306700
Desc
Variant0032
Relatedalso
ClinVar
Risk rs137852362(G;G)
Alt rs137852362(G;G)
Reference rs137852362(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.154156882T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010829.3,