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rs137852473

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852473(C;T)
Make rs137852473(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154837686
GeneF8
is asnp
is mentioned by
dbSNPrs137852473
ebirs137852473
HLIrs137852473
Exacrs137852473
Varsomers137852473
Maprs137852473
PheGenIrs137852473
hapmaprs137852473
1000 genomesrs137852473
hgdprs137852473
ensemblrs137852473
gopubmedrs137852473
geneviewrs137852473
scholarrs137852473
googlers137852473
pharmgkbrs137852473
gwascentralrs137852473
openSNPrs137852473
23andMers137852473
23andMe allrs137852473
SNP Nexus

SNPshotrs137852473
SNPdbers137852473
MSV3drs137852473
GWAS Ctlgrs137852473
Max Magnitude0
OMIM306700
Desc
Variant0250
Relatedalso
ClinVar
Risk rs137852473(T;T)
Alt rs137852473(T;T)
Reference rs137852473(C;C)
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.154065961G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011046.2,