Table 2 Age-related hearing loss-associated loci commonly identified in recent genome-wide association studies

rs36062310

chr22: 50549676

A

G

KLHDC7B

NM_138433.5; p.Val504Met

Missense variant

0.00009022

-

1.027

rs10901863

chr10:125123701

T

C

CTBP2

Intron variant

0.1782

-

1.011

rs5756795

chr22:37726115

C

T

TRIOBP

NM_001039141.3; p.Phe1187Leu

Missense variant

0.5642

0.603120

0.992

rs9493627

chr6:133468590

A

G

EYA4

NM_004100.5; p.Gly277Ser

Missense variant

0.3518

0.391820

1.009

rs67307131

chr11:118609508

C

T

PHLDB1

Intron variant

0.3099

-

0.992

rs11238325

chr7:50785454

C

T

GRB10

Intron variant

0.7107

0.711810

1.007

rs6545432

chr2:54590546

G

A

SPTBN1

Intron variant

0.4387

0.467130

1.007

rs7525101

chr1:165139894

T

C

LMX1A

Intergenic variant

0.6343

0.597030

1.006

rs143796236

chr17:81528943

T

C

FSCN2

NM_001077182.3; p.His138Tyr

Missense variant

0.00002277

-

1.035

rs13171669

chr5:149221680

G

A

ABLIM3

Intron variant

0.5945

0.556470

0.942

rs920701

chr13:75842965

C

T

LMO7

Intron variant

0.3611

0.354260

0.942

rs11881070

chr19:2389142

T

C

TMPRSS9

Upstream gene variant

0.5452

0.563680

0.942

rs143282422

chr10:71617355

A

G

CDH23

NM_022124.6; p.Ala366Thr

Missense variant

0.00004456

-

1.032