Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852505

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852505(G;G)
Make rs137852505(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position134493564
GeneHPRT1
is asnp
is mentioned by
dbSNPrs137852505
ebirs137852505
HLIrs137852505
Exacrs137852505
Varsomers137852505
Maprs137852505
PheGenIrs137852505
hapmaprs137852505
1000 genomesrs137852505
hgdprs137852505
ensemblrs137852505
gopubmedrs137852505
geneviewrs137852505
scholarrs137852505
googlers137852505
pharmgkbrs137852505
gwascentralrs137852505
openSNPrs137852505
23andMers137852505
23andMe allrs137852505
SNP Nexus

SNPshotrs137852505
SNPdbers137852505
MSV3drs137852505
GWAS Ctlgrs137852505
Max Magnitude0
OMIM308000
Desc
Variant0057
Relatedalso
ClinVar
Risk rs137852505(G;G)
Alt rs137852505(G;G)
Reference rs137852505(T;T)
Significance Other
Disease Lesch-Nyhan syndrome HPRT PARIS
Variation info
Gene HPRT1
CLNDBN Lesch-Nyhan syndrome HPRT PARIS
Reversed 0
HGVS NC_000023.10:g.133627594T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010793.4, RCV000010794.1,