Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75759941
RPGR
0.925 0.080 X 38291789 intron variant T/C snv 7.5E-02 2
rs7048567
ABCA2
1.000 9 137009585 synonymous variant A/G snv 0.68 0.70 1
rs7087342
ADARB2
1.000 10 1613599 intron variant G/A snv 0.11 1
rs78512431
AGPAT3
1.000 21 43970856 intron variant T/A;C snv 0.10 1
rs77063336
ASTN2
1.000 9 116932295 intron variant C/T snv 3.3E-02 1
rs151068302
CAAP1
1.000 9 26883048 intron variant C/T snv 6.1E-02 1
rs184429573
CCDC91
1.000 12 28504235 intron variant A/C snv 9.1E-03 1
rs192238733
CELF2
1.000 10 11109944 intron variant G/A snv 4.1E-03 1
rs116264298
CENPC
1.000 4 67496237 intron variant T/C snv 1.7E-02 1
rs180822335
COL13A1
1.000 10 69950109 intron variant T/C snv 5.9E-03 1
rs10505380
COL14A1
1.000 8 120314234 intron variant A/G snv 0.14 1
rs2267078
CRYBB2
1.000 22 25220484 intron variant T/A snv 9.9E-02 1
rs149325996
CTDP1
1.000 18 79735872 non coding transcript exon variant G/A snv 1.0E-02 1
rs75495219
CTNNA3
1.000 10 67151138 intron variant A/G snv 6.0E-02 1
rs72656469
CYP7B1
1.000 8 64701356 intron variant C/T snv 1.9E-02 1
rs114830967
DPP10
1.000 2 115820465 intron variant C/T snv 2.0E-02 1
rs34180124
EHD4
1.000 15 41908697 non coding transcript exon variant T/A snv 2.7E-02 1
rs57997684
ELOVL2
1.000 6 11014323 intron variant A/C snv 0.13 1
rs150859230
ESRRG
1.000 1 216675108 intron variant C/T snv 1.4E-02 1
rs116502295
ETS1
1.000 11 128462620 intron variant T/C snv 6.1E-03 7.1E-03 1
rs211437
EYA4
1.000 6 133292270 intron variant T/C snv 4.0E-02 1
rs142630661
FAM86C1 ; ALG1L9P
1.000 11 71794579 non coding transcript exon variant C/G snv 1.3E-02 1
rs7721607
FBXL7
1.000 5 15652449 intron variant G/A snv 0.17 1
rs1790634
FHOD3
1.000 18 36419450 intron variant G/A snv 0.58 1
rs192597095
GLS2
1.000 12 56486375 intron variant C/T snv 8.6E-03 1