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rs863225072

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225072(G;G)
Make rs863225072(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position10019000
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs863225072
ebirs863225072
HLIrs863225072
Exacrs863225072
Varsomers863225072
Maprs863225072
PheGenIrs863225072
hapmaprs863225072
1000 genomesrs863225072
hgdprs863225072
ensemblrs863225072
gopubmedrs863225072
geneviewrs863225072
scholarrs863225072
googlers863225072
pharmgkbrs863225072
gwascentralrs863225072
openSNPrs863225072
23andMers863225072
23andMe allrs863225072
SNP Nexus

SNPshotrs863225072
SNPdbers863225072
MSV3drs863225072
GWAS Ctlgrs863225072
Max Magnitude0
ClinVar
Risk rs863225072(G;G)
Alt rs863225072(G;G)
Reference rs863225072(T;T)
Significance Pathogenic
Disease Renal hypouricemia 2
Variation info
Gene SLC2A9
CLNDBN Renal hypouricemia 2
Reversed 1
HGVS NC_000004.11:g.10020624A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000201282.1,