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rs137852437

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852437(C;T)
Make rs137852437(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154931350
GeneF8
is asnp
is mentioned by
dbSNPrs137852437
ebirs137852437
HLIrs137852437
Exacrs137852437
Varsomers137852437
Maprs137852437
PheGenIrs137852437
hapmaprs137852437
1000 genomesrs137852437
hgdprs137852437
ensemblrs137852437
gopubmedrs137852437
geneviewrs137852437
scholarrs137852437
googlers137852437
pharmgkbrs137852437
gwascentralrs137852437
openSNPrs137852437
23andMers137852437
23andMe allrs137852437
SNP Nexus

SNPshotrs137852437
SNPdbers137852437
MSV3drs137852437
GWAS Ctlgrs137852437
Max Magnitude0
OMIM306700
Desc
Variant0165
Relatedalso
ClinVar
Risk rs137852437(T;T)
Alt rs137852437(T;T)
Reference Rs137852437(C;C)
Significance Probable-Pathogenic
Disease Hereditary factor VIII deficiency disease
Variation info
Gene F8
CLNDBN Hereditary factor VIII deficiency disease
Reversed 1
HGVS NC_000023.10:g.154159625G>A
CLNSRC
CLNACC