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

rs181509591

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs181509591(A;A)
Make rs181509591(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position9996817
GeneLOC105374476, SLC2A9
is asnp
is mentioned by
dbSNPrs181509591
ebirs181509591
HLIrs181509591
Exacrs181509591
Varsomers181509591
Maprs181509591
PheGenIrs181509591
hapmaprs181509591
1000 genomesrs181509591
hgdprs181509591
ensemblrs181509591
gopubmedrs181509591
geneviewrs181509591
scholarrs181509591
googlers181509591
pharmgkbrs181509591
gwascentralrs181509591
openSNPrs181509591
23andMers181509591
23andMe allrs181509591
SNP Nexus

SNPshotrs181509591
SNPdbers181509591
MSV3drs181509591
GWAS Ctlgrs181509591
Max Magnitude0
ClinVar
Risk rs181509591(A,C;A,C)
Alt rs181509591(A,C;A,C)
Reference rs181509591(G;G)
Significance Pathogenic
Disease Renal hypouricemia 2
Variation info
Gene SLC2A9
CLNDBN Renal hypouricemia 2
Reversed 0
HGVS NC_000004.11:g.9998441G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201283.1,