rs1869026

Orientation

minus

Stabilized

minus

Make rs1869026(G;G)

Make rs1869026(G;T)

Make rs1869026(T;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

120583705

is a	snp
is	mentioned by
dbSNP	rs1869026
dbSNP (classic)	rs1869026
ClinGen	rs1869026
ebi	rs1869026
HLI	rs1869026
Exac	rs1869026
Gnomad	rs1869026
Varsome	rs1869026
LitVar	rs1869026
Map	rs1869026
PheGenI	rs1869026
Biobank	rs1869026
1000 genomes	rs1869026
hgdp	rs1869026
ensembl	rs1869026
geneview	rs1869026
scholar	rs1869026
google	rs1869026
pharmgkb	rs1869026
gwascentral	rs1869026
openSNP	rs1869026
23andMe	rs1869026
SNPshot	rs1869026
SNPdbe	rs1869026
MSV3d	rs1869026
GWAS Ctlg	rs1869026

Max Magnitude

0

?	(G;G) (G;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	4E-10
Odds Ratio	NR NR