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rs137852503

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852503(A;A)
Make rs137852503(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position134493524
GeneHPRT1
is asnp
is mentioned by
dbSNPrs137852503
ebirs137852503
HLIrs137852503
Exacrs137852503
Varsomers137852503
Maprs137852503
PheGenIrs137852503
hapmaprs137852503
1000 genomesrs137852503
hgdprs137852503
ensemblrs137852503
gopubmedrs137852503
geneviewrs137852503
scholarrs137852503
googlers137852503
pharmgkbrs137852503
gwascentralrs137852503
openSNPrs137852503
23andMers137852503
23andMe allrs137852503
SNP Nexus

SNPshotrs137852503
SNPdbers137852503
MSV3drs137852503
GWAS Ctlgrs137852503
Max Magnitude0
OMIM308000
Desc
Variant0055
Relatedalso
ClinVar
Risk rs137852503(A;A)
Alt rs137852503(A;A)
Reference rs137852503(G;G)
Significance Other
Disease Lesch-Nyhan syndrome HPRT TOKYO
Variation info
Gene HPRT1
CLNDBN Lesch-Nyhan syndrome HPRT TOKYO
Reversed 0
HGVS NC_000023.10:g.133627554G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010789.2, RCV000010790.1,