rs6706649
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6706649(C;C) |
Make rs6706649(C;T) |
Make rs6706649(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 177265343 |
Gene | NFE2L2 |
is a | snp |
is | mentioned by |
dbSNP | rs6706649 |
dbSNP (classic) | rs6706649 |
ClinGen | rs6706649 |
ebi | rs6706649 |
HLI | rs6706649 |
Exac | rs6706649 |
Gnomad | rs6706649 |
Varsome | rs6706649 |
LitVar | rs6706649 |
Map | rs6706649 |
PheGenI | rs6706649 |
Biobank | rs6706649 |
1000 genomes | rs6706649 |
hgdp | rs6706649 |
ensembl | rs6706649 |
geneview | rs6706649 |
scholar | rs6706649 |
rs6706649 | |
pharmgkb | rs6706649 |
gwascentral | rs6706649 |
openSNP | rs6706649 |
23andMe | rs6706649 |
SNPshot | rs6706649 |
SNPdbe | rs6706649 |
MSV3d | rs6706649 |
GWAS Ctlg | rs6706649 |
GMAF | 0.07805 |
Max Magnitude | 0 |
[PMID 22668754] Polymorphisms in the transcription factor NRF2 and forearm vasodilator responses in humans
[PMID 20196834] Association of Nrf2-encoding NFE2L2 haplotypes with Parkinson's disease.
[PMID 23176750] Genetic analysis of NFE2L2 promoter variation in Taiwanese Parkinson's disease