Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117893233 5 1041318 downstream gene variant C/T snv 2.6E-03 2
rs11774829
ZFPM2
8 104966140 intron variant T/A snv 7.6E-02 3
rs10991473 9 105024605 downstream gene variant G/A;C snv 2
rs12151021
ABCA7
19 1050875 intron variant A/G;T snv 0.69 3
rs55861694
SLC12A7
5 1051642 3 prime UTR variant A/C snv 1.1E-02 2
rs7252007
AP1M2
19 10577081 intron variant T/C snv 0.90 2
rs111910553
SLC12A7
5 1058272 intron variant G/A snv 1.1E-02 2
rs2360748
AP1M2
19 10582948 intron variant T/C snv 0.25 2
rs2885056
AP1M2
19 10582952 intron variant C/A;T snv 2
rs9486370
LOC101927405 ; CRYBG1
6 106494519 intron variant G/A;C snv 2
rs112694389
SLC12A7
5 1067827 intron variant C/T snv 5.1E-04 2
rs2232016
PRMT6
1 107057296 missense variant C/A;G;T snv 4.0E-06; 0.18 2
rs10099100 8 10719265 downstream gene variant G/C snv 0.32 3
rs112665932
COG5
7 107275676 intron variant A/G snv 0.13 2
rs11133613
SLC12A7
5 1074936 intron variant A/G snv 0.91 2
rs11952124
SLC12A7
5 1076344 intron variant G/T snv 0.72 2
rs1967604
LOC105376208 ; LOC105376209
9 107768043 regulatory region variant A/G snv 0.77 2
rs113084827
DNM2
19 10807681 intron variant G/A;T snv 2
rs634454
LOC105376214
9 108150874 regulatory region variant T/G snv 0.86 2
rs141839244
SLC12A7
5 1085619 intron variant C/T snv 8.9E-03 2
rs193104780 6 108775380 intergenic variant G/A snv 4.7E-03 2
rs200980971
CCDC162P
6 109261139 intron variant A/-;AA delins 2
rs36052053
CCDC162P
6 109262596 intron variant G/A snv 0.11 2
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs6568570
CCDC162P
6 109292038 intron variant T/A;C;G snv 2