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rs16899974

From SNPedia

Orientationplus
Stabilizedplus
Make rs16899974(A;A)
Make rs16899974(A;C)
Make rs16899974(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position34998772
GeneAGXT2
is asnp
is mentioned by
dbSNPrs16899974
ebirs16899974
HLIrs16899974
Exacrs16899974
Varsomers16899974
Maprs16899974
PheGenIrs16899974
hapmaprs16899974
1000 genomesrs16899974
hgdprs16899974
ensemblrs16899974
gopubmedrs16899974
geneviewrs16899974
scholarrs16899974
googlers16899974
pharmgkbrs16899974
gwascentralrs16899974
openSNPrs16899974
23andMers16899974
23andMe allrs16899974
SNP Nexus

SNPshotrs16899974
SNPdbers16899974
MSV3drs16899974
GWAS Ctlgrs16899974
GMAF0.2383
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 24159190] Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality


[PMID 25620171] Missense variants of the alanine: glyoxylate aminotransferase 2 gene correlated with carotid atherosclerosis in the Japanese population