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rs137852458

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852458(G;G)
Make rs137852458(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154896146
GeneF8
is asnp
is mentioned by
dbSNPrs137852458
ebirs137852458
HLIrs137852458
Exacrs137852458
Varsomers137852458
Maprs137852458
PheGenIrs137852458
hapmaprs137852458
1000 genomesrs137852458
hgdprs137852458
ensemblrs137852458
gopubmedrs137852458
geneviewrs137852458
scholarrs137852458
googlers137852458
pharmgkbrs137852458
gwascentralrs137852458
openSNPrs137852458
23andMers137852458
23andMe allrs137852458
SNP Nexus

SNPshotrs137852458
SNPdbers137852458
MSV3drs137852458
GWAS Ctlgrs137852458
Max Magnitude0
OMIM306700
Desc
Variant0226
Relatedalso
ClinVar
Risk rs137852458(G;G)
Alt rs137852458(G;G)
Reference rs137852458(T;T)
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.154124421A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011022.4,