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rs1488564

From SNPedia

Orientationplus
Stabilizedplus
Make rs1488564(A;A)
Make rs1488564(A;G)
Make rs1488564(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position173736078
GeneNLGN1
is asnp
is mentioned by
dbSNPrs1488564
ebirs1488564
HLIrs1488564
Exacrs1488564
Varsomers1488564
Maprs1488564
PheGenIrs1488564
hapmaprs1488564
1000 genomesrs1488564
hgdprs1488564
ensemblrs1488564
gopubmedrs1488564
geneviewrs1488564
scholarrs1488564
googlers1488564
pharmgkbrs1488564
gwascentralrs1488564
openSNPrs1488564
23andMers1488564
23andMe allrs1488564
SNP Nexus

SNPshotrs1488564
SNPdbers1488564
MSV3drs1488564
GWAS Ctlgrs1488564
Max Magnitude
? (A;A) (A;G) (G;G) 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 8E-9
Odds Ratio NR NR