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rs137852486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852486(G;G)
Make rs137852486(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position134498670
GeneHPRT1
is asnp
is mentioned by
dbSNPrs137852486
ebirs137852486
HLIrs137852486
Exacrs137852486
Varsomers137852486
Maprs137852486
PheGenIrs137852486
hapmaprs137852486
1000 genomesrs137852486
hgdprs137852486
ensemblrs137852486
gopubmedrs137852486
geneviewrs137852486
scholarrs137852486
googlers137852486
pharmgkbrs137852486
gwascentralrs137852486
openSNPrs137852486
23andMers137852486
23andMe allrs137852486
SNP Nexus

SNPshotrs137852486
SNPdbers137852486
MSV3drs137852486
GWAS Ctlgrs137852486
Max Magnitude0
OMIM308000
Desc
Variant0015
Relatedalso
ClinVar
Risk rs137852486(G;G)
Alt rs137852486(G;G)
Reference rs137852486(T;T)
Significance Other
Disease Lesch-Nyhan syndrome HPRT NEW BRITON
Variation info
Gene HPRT1
CLNDBN Lesch-Nyhan syndrome HPRT NEW BRITON
Reversed 0
HGVS NC_000023.10:g.133632700T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010740.2, RCV000010741.1,