rs10916814

Orientation

plus

Stabilized

plus

Make rs10916814(C;C)

Make rs10916814(C;T)

Make rs10916814(T;T)

Reference

GRCh38 38.1/142

Chromosome

1

Position

20566438

is a	snp
is	mentioned by
dbSNP	rs10916814
dbSNP (classic)	rs10916814
ClinGen	rs10916814
ebi	rs10916814
HLI	rs10916814
Exac	rs10916814
Gnomad	rs10916814
Varsome	rs10916814
LitVar	rs10916814
Map	rs10916814
PheGenI	rs10916814
Biobank	rs10916814
1000 genomes	rs10916814
hgdp	rs10916814
ensembl	rs10916814
geneview	rs10916814
scholar	rs10916814
google	rs10916814
pharmgkb	rs10916814
gwascentral	rs10916814
openSNP	rs10916814
23andMe	rs10916814
SNPshot	rs10916814
SNPdbe	rs10916814
MSV3d	rs10916814
GWAS Ctlg	rs10916814

Max Magnitude

0

?	(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	5E-10
Odds Ratio	NR NR