Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51 4
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs6012558 20 48914749 intergenic variant G/A snv 0.42 4
rs61754230
RAB21
12 71785666 missense variant C/T snv 1.3E-02 1.2E-02 4
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 4
rs1007934
ZFYVE1
14 72996771 intron variant G/A snv 0.33 3
rs11209951
LOC105378797
1 72371807 intron variant C/T snv 0.61 3
rs1541374 4 105127203 intergenic variant T/A;G snv 3
rs2008514 16 28814284 non coding transcript exon variant G/A snv 0.35 3
rs2013208
RBM5 ; RBM6
3 50091966 intron variant C/T snv 0.61 0.56 3
rs2302190
MTMR4
17 58507147 missense variant T/A;C snv 0.24 3
rs2393967
MIR1296 ; JMJD1C
10 63373396 intron variant A/C snv 0.23 3
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs475616 10 30207976 regulatory region variant A/G snv 0.67 3
rs6731373
LOC107985892
2 68275912 intergenic variant G/A snv 0.29 3
rs707938
MSH5-SAPCD1 ; MSH5 ; SAPCD1
6 31761582 synonymous variant A/G snv 0.38 0.44 3
rs7924036
JMJD1C
10 63431885 intron variant G/A;T snv 3
rs7963801
SYT1
12 79291446 intron variant T/C snv 0.70 3
rs901630 6 98091643 intron variant C/T snv 0.32 3
rs916888
LRRC37A2 ; WNT3
17 46785767 intron variant T/C snv 0.19 3
rs974471
LOC102724934
14 29216122 intron variant G/A snv 0.74 3
rs9906944
IGF2BP1
17 49014058 intron variant C/G;T snv 3
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2