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rs137852487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852487(A;A)
Make rs137852487(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position134475255
GeneHPRT1
is asnp
is mentioned by
dbSNPrs137852487
ebirs137852487
HLIrs137852487
Exacrs137852487
Varsomers137852487
Maprs137852487
PheGenIrs137852487
hapmaprs137852487
1000 genomesrs137852487
hgdprs137852487
ensemblrs137852487
gopubmedrs137852487
geneviewrs137852487
scholarrs137852487
googlers137852487
pharmgkbrs137852487
gwascentralrs137852487
openSNPrs137852487
23andMers137852487
23andMe allrs137852487
SNP Nexus

SNPshotrs137852487
SNPdbers137852487
MSV3drs137852487
GWAS Ctlgrs137852487
Max Magnitude0
OMIM308000
Desc
Variant0016
Relatedalso
ClinVar
Risk rs137852487(A;A)
Alt rs137852487(A;A)
Reference rs137852487(G;G)
Significance Other
Disease Lesch-Nyhan syndrome HPRT NEW HAVEN
Variation info
Gene HPRT1
CLNDBN Lesch-Nyhan syndrome HPRT NEW HAVEN
Reversed 0
HGVS NC_000023.10:g.133609285G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010742.2, RCV000010743.1,