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rs7331194

From SNPedia

Orientationplus
Stabilizedplus
Make rs7331194(C;C)
Make rs7331194(C;G)
Make rs7331194(G;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position105448044
is asnp
is mentioned by
dbSNPrs7331194
ebirs7331194
HLIrs7331194
Exacrs7331194
Varsomers7331194
Maprs7331194
PheGenIrs7331194
hapmaprs7331194
1000 genomesrs7331194
hgdprs7331194
ensemblrs7331194
gopubmedrs7331194
geneviewrs7331194
scholarrs7331194
googlers7331194
pharmgkbrs7331194
gwascentralrs7331194
openSNPrs7331194
23andMers7331194
23andMe allrs7331194
SNP Nexus

SNPshotrs7331194
SNPdbers7331194
MSV3drs7331194
GWAS Ctlgrs7331194
Max Magnitude
? (C;C) (C;G) (G;G) 28
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 4E-6
Odds Ratio .06 [NR] unit increase