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rs9366664

From SNPedia

Orientationplus
Stabilizedplus
Make rs9366664(C;C)
Make rs9366664(C;T)
Make rs9366664(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position10892266
GeneSYCP2L
is asnp
is mentioned by
dbSNPrs9366664
ebirs9366664
HLIrs9366664
Exacrs9366664
Varsomers9366664
Maprs9366664
PheGenIrs9366664
hapmaprs9366664
1000 genomesrs9366664
hgdprs9366664
ensemblrs9366664
gopubmedrs9366664
geneviewrs9366664
scholarrs9366664
googlers9366664
pharmgkbrs9366664
gwascentralrs9366664
openSNPrs9366664
23andMers9366664
23andMe allrs9366664
SNP Nexus

SNPshotrs9366664
SNPdbers9366664
MSV3drs9366664
GWAS Ctlgrs9366664
Max Magnitude
? (C;C) (C;T) (T;T) 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 1E-9
Odds Ratio NR NR