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rs4301303

From SNPedia

Orientationplus
Stabilizedplus
Make rs4301303(C;C)
Make rs4301303(C;T)
Make rs4301303(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position40635318
is asnp
is mentioned by
dbSNPrs4301303
ebirs4301303
HLIrs4301303
Exacrs4301303
Varsomers4301303
Maprs4301303
PheGenIrs4301303
hapmaprs4301303
1000 genomesrs4301303
hgdprs4301303
ensemblrs4301303
gopubmedrs4301303
geneviewrs4301303
scholarrs4301303
googlers4301303
pharmgkbrs4301303
gwascentralrs4301303
openSNPrs4301303
23andMers4301303
23andMe allrs4301303
SNP Nexus

SNPshotrs4301303
SNPdbers4301303
MSV3drs4301303
GWAS Ctlgrs4301303
Max Magnitude
? (C;C) (C;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 7E-9
Odds Ratio NR NR