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rs10102392

From SNPedia

Orientationplus
Stabilizedplus
Make rs10102392(A;A)
Make rs10102392(A;G)
Make rs10102392(G;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position85555309
is asnp
is mentioned by
dbSNPrs10102392
ebirs10102392
HLIrs10102392
Exacrs10102392
Varsomers10102392
Maprs10102392
PheGenIrs10102392
hapmaprs10102392
1000 genomesrs10102392
hgdprs10102392
ensemblrs10102392
gopubmedrs10102392
geneviewrs10102392
scholarrs10102392
googlers10102392
pharmgkbrs10102392
gwascentralrs10102392
openSNPrs10102392
23andMers10102392
23andMe allrs10102392
SNP Nexus

SNPshotrs10102392
SNPdbers10102392
MSV3drs10102392
GWAS Ctlgrs10102392
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 7E-9
Odds Ratio NR NR