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rs17170356

From SNPedia

Orientationplus
Stabilizedplus
Make rs17170356(A;A)
Make rs17170356(A;G)
Make rs17170356(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position147190776
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs17170356
ebirs17170356
HLIrs17170356
Exacrs17170356
Varsomers17170356
Maprs17170356
PheGenIrs17170356
hapmaprs17170356
1000 genomesrs17170356
hgdprs17170356
ensemblrs17170356
gopubmedrs17170356
geneviewrs17170356
scholarrs17170356
googlers17170356
pharmgkbrs17170356
gwascentralrs17170356
openSNPrs17170356
23andMers17170356
23andMe allrs17170356
SNP Nexus

SNPshotrs17170356
SNPdbers17170356
MSV3drs17170356
GWAS Ctlgrs17170356
Max Magnitude
? (A;A) (A;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 .15 [NR] unit increase