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rs7816613

From SNPedia

Orientationplus
Stabilizedplus
Make rs7816613(C;C)
Make rs7816613(C;T)
Make rs7816613(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position101717247
GeneNCALD
is asnp
is mentioned by
dbSNPrs7816613
ebirs7816613
HLIrs7816613
Exacrs7816613
Varsomers7816613
Maprs7816613
PheGenIrs7816613
hapmaprs7816613
1000 genomesrs7816613
hgdprs7816613
ensemblrs7816613
gopubmedrs7816613
geneviewrs7816613
scholarrs7816613
googlers7816613
pharmgkbrs7816613
gwascentralrs7816613
openSNPrs7816613
23andMers7816613
23andMe allrs7816613
SNP Nexus

SNPshotrs7816613
SNPdbers7816613
MSV3drs7816613
GWAS Ctlgrs7816613
Max Magnitude
? (C;C) (C;T) (T;T) 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 8E-6
Odds Ratio .14 [NR] unit increase