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rs1494630

From SNPedia

Orientationminus
Stabilizedminus
Make rs1494630(C;C)
Make rs1494630(C;T)
Make rs1494630(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position64098343
is asnp
is mentioned by
dbSNPrs1494630
ebirs1494630
HLIrs1494630
Exacrs1494630
Varsomers1494630
Maprs1494630
PheGenIrs1494630
hapmaprs1494630
1000 genomesrs1494630
hgdprs1494630
ensemblrs1494630
gopubmedrs1494630
geneviewrs1494630
scholarrs1494630
googlers1494630
pharmgkbrs1494630
gwascentralrs1494630
openSNPrs1494630
23andMers1494630
23andMe allrs1494630
SNP Nexus

SNPshotrs1494630
SNPdbers1494630
MSV3drs1494630
GWAS Ctlgrs1494630
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 1E-6
Odds Ratio .15 [NR] unit decrease