rs10102392

Orientation

plus

Stabilized

plus

Make rs10102392(A;A)

Make rs10102392(A;G)

Make rs10102392(G;G)

Reference

GRCh38 38.1/142

Chromosome

8

Position

85555309

is a	snp
is	mentioned by
dbSNP	rs10102392
dbSNP (classic)	rs10102392
ClinGen	rs10102392
ebi	rs10102392
HLI	rs10102392
Exac	rs10102392
Gnomad	rs10102392
Varsome	rs10102392
LitVar	rs10102392
Map	rs10102392
PheGenI	rs10102392
Biobank	rs10102392
1000 genomes	rs10102392
hgdp	rs10102392
ensembl	rs10102392
geneview	rs10102392
scholar	rs10102392
google	rs10102392
pharmgkb	rs10102392
gwascentral	rs10102392
openSNP	rs10102392
23andMe	rs10102392
SNPshot	rs10102392
SNPdbe	rs10102392
MSV3d	rs10102392
GWAS Ctlg	rs10102392

Max Magnitude

0

?	(A;A) (A;G) (G;G)	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	7E-9
Odds Ratio	NR NR