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

rs12704795

From SNPedia

Orientationplus
Stabilizedplus
Make rs12704795(G;G)
Make rs12704795(G;T)
Make rs12704795(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position95424695
GenePON2
is asnp
is mentioned by
dbSNPrs12704795
ebirs12704795
HLIrs12704795
Exacrs12704795
Varsomers12704795
Maprs12704795
PheGenIrs12704795
hapmaprs12704795
1000 genomesrs12704795
hgdprs12704795
ensemblrs12704795
gopubmedrs12704795
geneviewrs12704795
scholarrs12704795
googlers12704795
pharmgkbrs12704795
gwascentralrs12704795
openSNPrs12704795
23andMers12704795
23andMe allrs12704795
SNP Nexus

SNPshotrs12704795
SNPdbers12704795
MSV3drs12704795
GWAS Ctlgrs12704795
Merged fromRs17876088
GMAF0.225
Max Magnitude
According to [PMID 16822964], variations at rs12704795, originally known as rs17876088, located in an intron of the PON2 gene, appear to modulate both susceptibility to, and protection from, the sporadic form of ALS (Lou Gehrig's disease).
Neighborrs17876088
Distance1

[PMID 17096118] Paraoxonase 2 (PON2) polymorphisms and development of renal dysfunction in type 2 diabetes: UKPDS 76.

[PMID 19546579OA-icon.png] Evaluation of polymorphisms in paraoxonase 2 (PON2) gene and their association with cardiovascular-renal disease risk in Mexican Americans.

[PMID 21223581OA-icon.png] Association analysis of PON2 genetic variants with serum paraoxonase activity and systemic lupus erythematosus.