Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs34338164
PLEK
2 68388414 missense variant A/C snv 8.0E-03 7.8E-03 4
rs56232812 1 27859995 intergenic variant A/C snv 0.11 4
rs4805881
PEPD
19 33405526 intron variant A/C snv 0.69 3
rs17041439
SPIC
12 101479462 intron variant A/C snv 7.0E-02 2
rs77940566 6 42542864 intergenic variant A/C snv 0.21 2
rs1016680 17 37514283 downstream gene variant A/C snv 0.74 1
rs10273974
ZC3HAV1
7 139050766 intron variant A/C snv 0.48 1
rs113164910 6 32459228 downstream gene variant A/C snv 1
rs12130298
CD101
1 117001709 upstream gene variant A/C snv 5.0E-02 1
rs17088512
DACH1
13 71832596 intron variant A/C snv 9.2E-02 1
rs35990176 21 43052008 downstream gene variant A/C snv 1
rs3747869
VSIR ; CDH23
10 71760875 missense variant A/C snv 0.88 0.90 1
rs3845624 1 159248476 regulatory region variant A/C snv 0.57 1
rs4281320 1 26147948 regulatory region variant A/C snv 0.14 1
rs59667935
CECR2
22 17427131 intron variant A/C snv 0.15 1
rs6672992
DNAJC6
1 65382351 intron variant A/C snv 0.12 1
rs72675531
LOC105378741
1 56111740 intergenic variant A/C snv 0.26 1
rs75859969 16 50126826 intron variant A/C snv 0.17 1
rs76721774
CUX2
12 111268872 intron variant A/C snv 1.1E-02 1
rs77696237
CDH12
5 22076380 intron variant A/C snv 1.9E-02 1
rs78784853
TXNDC11
16 11723610 intron variant A/C snv 6.4E-02 1
rs8085287
RBBP8
18 22884208 intron variant A/C snv 0.68 1