Have questions? Visit https://www.reddit.com/r/SNPedia

rs2197609

From SNPedia

Orientationminus
Stabilizedminus
Make rs2197609(A;A)
Make rs2197609(A;C)
Make rs2197609(C;C)
ReferenceGRCh38 38.1/142
Chromosome13
Position84603753
is asnp
is mentioned by
dbSNPrs2197609
ebirs2197609
HLIrs2197609
Exacrs2197609
Varsomers2197609
Maprs2197609
PheGenIrs2197609
hapmaprs2197609
1000 genomesrs2197609
hgdprs2197609
ensemblrs2197609
gopubmedrs2197609
geneviewrs2197609
scholarrs2197609
googlers2197609
pharmgkbrs2197609
gwascentralrs2197609
openSNPrs2197609
23andMers2197609
23andMe allrs2197609
SNP Nexus

SNPshotrs2197609
SNPdbers2197609
MSV3drs2197609
GWAS Ctlgrs2197609
Max Magnitude
? (A;A) (A;C) (C;C) 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 2E-9
Odds Ratio NR NR