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rs1320851

From SNPedia

Orientationplus
Stabilizedplus
Make rs1320851(G;G)
Make rs1320851(G;T)
Make rs1320851(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position66048174
is asnp
is mentioned by
dbSNPrs1320851
ebirs1320851
HLIrs1320851
Exacrs1320851
Varsomers1320851
Maprs1320851
PheGenIrs1320851
hapmaprs1320851
1000 genomesrs1320851
hgdprs1320851
ensemblrs1320851
gopubmedrs1320851
geneviewrs1320851
scholarrs1320851
googlers1320851
pharmgkbrs1320851
gwascentralrs1320851
openSNPrs1320851
23andMers1320851
23andMe allrs1320851
SNP Nexus

SNPshotrs1320851
SNPdbers1320851
MSV3drs1320851
GWAS Ctlgrs1320851
Max Magnitude
? (G;G) (G;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 9E-9
Odds Ratio NR NR