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rs371713160

From SNPedia

Orientationplus
Stabilizedplus
Make rs371713160(A;A)
Make rs371713160(A;G)
Make rs371713160(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position12379690
GenePPARG
is asnp
is mentioned by
dbSNPrs371713160
dbSNP (classic)rs371713160
ClinGenrs371713160
ebirs371713160
HLIrs371713160
Exacrs371713160
Gnomadrs371713160
Varsomers371713160
LitVarrs371713160
Maprs371713160
PheGenIrs371713160
Biobankrs371713160
1000 genomesrs371713160
hgdprs371713160
ensemblrs371713160
geneviewrs371713160
scholarrs371713160
googlers371713160
pharmgkbrs371713160
gwascentralrs371713160
openSNPrs371713160
23andMers371713160
23andMe allrs371713160
SNPshotrs371713160
SNPdbers371713160
MSV3drs371713160
GWAS Ctlgrs371713160
Max Magnitude0

[PMID 27569544OA-icon.png] 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.