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rs7786410

From SNPedia

Orientationplus
Stabilizedplus
Make rs7786410(A;A)
Make rs7786410(A;G)
Make rs7786410(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position55854630
GeneSEPT14
is asnp
is mentioned by
dbSNPrs7786410
ebirs7786410
HLIrs7786410
Exacrs7786410
Varsomers7786410
Maprs7786410
PheGenIrs7786410
hapmaprs7786410
1000 genomesrs7786410
hgdprs7786410
ensemblrs7786410
gopubmedrs7786410
geneviewrs7786410
scholarrs7786410
googlers7786410
pharmgkbrs7786410
gwascentralrs7786410
openSNPrs7786410
23andMers7786410
23andMe allrs7786410
SNP Nexus

SNPshotrs7786410
SNPdbers7786410
MSV3drs7786410
GWAS Ctlgrs7786410
Max Magnitude
GWAS snp
PMID [PMID 24939585]
Trait Age-related hearing impairment
Title Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.
Risk Allele
P-val 8E-6
Odds Ratio .15 [NR] unit decrease