rs787274

Orientation

plus

Stabilized

plus

Make rs787274(A;A)

Make rs787274(A;C)

Make rs787274(C;C)

Reference

GRCh38 38.1/142

Chromosome

9

Position

112788083

Gene

SNX30

is a	snp
is	mentioned by
dbSNP	rs787274
dbSNP (classic)	rs787274
ClinGen	rs787274
ebi	rs787274
HLI	rs787274
Exac	rs787274
Gnomad	rs787274
Varsome	rs787274
LitVar	rs787274
Map	rs787274
PheGenI	rs787274
Biobank	rs787274
1000 genomes	rs787274
hgdp	rs787274
ensembl	rs787274
geneview	rs787274
scholar	rs787274
google	rs787274
pharmgkb	rs787274
gwascentral	rs787274
openSNP	rs787274
23andMe	rs787274
SNPshot	rs787274
SNPdbe	rs787274
MSV3d	rs787274
GWAS Ctlg	rs787274

Max Magnitude

0

?	(A;A) (A;C) (C;C)	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-10
Odds Ratio	NR NR