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rs62459614

From SNPedia

Orientationplus
Stabilizedplus
Make rs62459614(C;C)
Make rs62459614(C;T)
Make rs62459614(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position71122159
is asnp
is mentioned by
dbSNPrs62459614
ebirs62459614
HLIrs62459614
Exacrs62459614
Varsomers62459614
Maprs62459614
PheGenIrs62459614
hapmaprs62459614
1000 genomesrs62459614
hgdprs62459614
ensemblrs62459614
gopubmedrs62459614
geneviewrs62459614
scholarrs62459614
googlers62459614
pharmgkbrs62459614
gwascentralrs62459614
openSNPrs62459614
23andMers62459614
23andMe allrs62459614
SNP Nexus

SNPshotrs62459614
SNPdbers62459614
MSV3drs62459614
GWAS Ctlgrs62459614
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 2E-6
Odds Ratio .19 [NR] unit increase