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rs180275

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
Make rs180275(C;T)
Make rs180275(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position93906158
GeneGNGT1
is asnp
is mentioned by
dbSNPrs180275
ebirs180275
HLIrs180275
Exacrs180275
Varsomers180275
Maprs180275
PheGenIrs180275
hapmaprs180275
1000 genomesrs180275
hgdprs180275
ensemblrs180275
gopubmedrs180275
geneviewrs180275
scholarrs180275
googlers180275
pharmgkbrs180275
gwascentralrs180275
openSNPrs180275
23andMers180275
23andMe allrs180275
SNP Nexus

SNPshotrs180275
SNPdbers180275
MSV3drs180275
GWAS Ctlgrs180275
GMAF0.0932
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 16280132] rs180275(G) associated with increased risk of sudden deafness in Korean population. odds ratio (OR) for SD associated with the G vs. A allele was 2.58

[PMID 18433792] rs180275 G allele protective against an increase in BMI in Korean population.