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rs7770227

From SNPedia

Orientationplus
Stabilizedplus
Make rs7770227(A;A)
Make rs7770227(A;G)
Make rs7770227(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position114301050
is asnp
is mentioned by
dbSNPrs7770227
ebirs7770227
HLIrs7770227
Exacrs7770227
Varsomers7770227
Maprs7770227
PheGenIrs7770227
hapmaprs7770227
1000 genomesrs7770227
hgdprs7770227
ensemblrs7770227
gopubmedrs7770227
geneviewrs7770227
scholarrs7770227
googlers7770227
pharmgkbrs7770227
gwascentralrs7770227
openSNPrs7770227
23andMers7770227
23andMe allrs7770227
SNP Nexus

SNPshotrs7770227
SNPdbers7770227
MSV3drs7770227
GWAS Ctlgrs7770227
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 5E-9
Odds Ratio NR NR