rs877674

Orientation

minus

Stabilized

minus

Make rs877674(C;C)

Make rs877674(C;T)

Make rs877674(T;T)

Reference

GRCh38 38.1/142

Chromosome

1

Position

31776605

is a	snp
is	mentioned by
dbSNP	rs877674
dbSNP (classic)	rs877674
ClinGen	rs877674
ebi	rs877674
HLI	rs877674
Exac	rs877674
Gnomad	rs877674
Varsome	rs877674
LitVar	rs877674
Map	rs877674
PheGenI	rs877674
Biobank	rs877674
1000 genomes	rs877674
hgdp	rs877674
ensembl	rs877674
geneview	rs877674
scholar	rs877674
google	rs877674
pharmgkb	rs877674
gwascentral	rs877674
openSNP	rs877674
23andMe	rs877674
SNPshot	rs877674
SNPdbe	rs877674
MSV3d	rs877674
GWAS Ctlg	rs877674

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	4E-11
Odds Ratio	NR NR