rs371713160
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs371713160(A;A) |
Make rs371713160(A;G) |
Make rs371713160(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 3 |
Position | 12379690 |
Gene | PPARG |
is a | snp |
is | mentioned by |
dbSNP | rs371713160 |
dbSNP (classic) | rs371713160 |
ClinGen | rs371713160 |
ebi | rs371713160 |
HLI | rs371713160 |
Exac | rs371713160 |
Gnomad | rs371713160 |
Varsome | rs371713160 |
LitVar | rs371713160 |
Map | rs371713160 |
PheGenI | rs371713160 |
Biobank | rs371713160 |
1000 genomes | rs371713160 |
hgdp | rs371713160 |
ensembl | rs371713160 |
geneview | rs371713160 |
scholar | rs371713160 |
rs371713160 | |
pharmgkb | rs371713160 |
gwascentral | rs371713160 |
openSNP | rs371713160 |
23andMe | rs371713160 |
SNPshot | rs371713160 |
SNPdbe | rs371713160 |
MSV3d | rs371713160 |
GWAS Ctlg | rs371713160 |
Max Magnitude | 0 |
[PMID 27569544] A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. This SNP maps to a position listed in Table S6 as a non-coding variant that their biocurators felt was convincingly associated with a Mendelian disease.