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rs2033711

From SNPedia

Orientationminus
Stabilizedminus
Make rs2033711(C;C)
Make rs2033711(C;T)
Make rs2033711(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position58487983
GeneZNF446
is asnp
is mentioned by
dbSNPrs2033711
dbSNP (old)rs2033711
ClinGenrs2033711
ebirs2033711
HLIrs2033711
Exacrs2033711
Gnomadrs2033711
Varsomers2033711
LitVarrs2033711
Maprs2033711
PheGenIrs2033711
Biobankrs2033711
1000 genomesrs2033711
hgdprs2033711
ensemblrs2033711
gopubmedrs2033711
geneviewrs2033711
scholarrs2033711
googlers2033711
pharmgkbrs2033711
gwascentralrs2033711
openSNPrs2033711
23andMers2033711
23andMe allrs2033711
SNPshotrs2033711
SNPdbers2033711
MSV3drs2033711
GWAS Ctlgrs2033711
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 28095793OA-icon.png] Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study.