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rs137852438

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852438(G;T)
Make rs137852438(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154928890
GeneF8
is asnp
is mentioned by
dbSNPrs137852438
ebirs137852438
HLIrs137852438
Exacrs137852438
Varsomers137852438
Maprs137852438
PheGenIrs137852438
hapmaprs137852438
1000 genomesrs137852438
hgdprs137852438
ensemblrs137852438
gopubmedrs137852438
geneviewrs137852438
scholarrs137852438
googlers137852438
pharmgkbrs137852438
gwascentralrs137852438
openSNPrs137852438
23andMers137852438
23andMe allrs137852438
SNP Nexus

SNPshotrs137852438
SNPdbers137852438
MSV3drs137852438
GWAS Ctlgrs137852438
Max Magnitude0
OMIM306700
Desc
Variant0182
Relatedalso
ClinVar
Risk rs137852438(T;T)
Alt rs137852438(T;T)
Reference rs137852438(G;G)
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.154157165C>A
CLNSRC
CLNACC