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rs787274

From SNPedia

Orientationplus
Stabilizedplus
Make rs787274(A;A)
Make rs787274(A;C)
Make rs787274(C;C)
ReferenceGRCh38 38.1/142
Chromosome9
Position112788083
GeneSNX30
is asnp
is mentioned by
dbSNPrs787274
ebirs787274
HLIrs787274
Exacrs787274
Varsomers787274
Maprs787274
PheGenIrs787274
hapmaprs787274
1000 genomesrs787274
hgdprs787274
ensemblrs787274
gopubmedrs787274
geneviewrs787274
scholarrs787274
googlers787274
pharmgkbrs787274
gwascentralrs787274
openSNPrs787274
23andMers787274
23andMe allrs787274
SNP Nexus

SNPshotrs787274
SNPdbers787274
MSV3drs787274
GWAS Ctlgrs787274
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24939585]
Trait Age-related hearing impairment (interaction)
Title Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.
Risk Allele
P-val 7E-10
Odds Ratio NR NR