rs17876088
From SNPedia
Merged into | rs12704795 |
Orientation | plus |
Stabilized | plus |
Make rs17876088(G;G) |
Make rs17876088(G;T) |
Make rs17876088(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 95424695 |
Gene | PON2 |
is a | snp |
is | mentioned by |
dbSNP | rs17876088 |
dbSNP (classic) | rs17876088 |
ClinGen | rs17876088 |
ebi | rs17876088 |
HLI | rs17876088 |
Exac | rs17876088 |
Gnomad | rs17876088 |
Varsome | rs17876088 |
LitVar | rs17876088 |
Map | rs17876088 |
PheGenI | rs17876088 |
Biobank | rs17876088 |
1000 genomes | rs17876088 |
hgdp | rs17876088 |
ensembl | rs17876088 |
geneview | rs17876088 |
scholar | rs17876088 |
rs17876088 | |
pharmgkb | rs17876088 |
gwascentral | rs17876088 |
openSNP | rs17876088 |
23andMe | rs17876088 |
SNPshot | rs17876088 |
SNPdbe | rs17876088 |
MSV3d | rs17876088 |
GWAS Ctlg | rs17876088 |
Status | Merged into rs12704795 |
Max Magnitude | 0 |
According to [PMID 16822964], variations at rs17876088, now known as rs12704795, 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).