Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7637773
IGF2BP2
1.000 0.080 3 185797847 intron variant G/A snv 0.38 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs3088050
NSD1
5 177299634 3 prime UTR variant G/A snv 0.18 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs6861681
CPEB4
5 173935455 intron variant G/A snv 0.22 1
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs2076529
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2
rs634869 6 139510620 intron variant T/A;C snv 2
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs1034207 6 127016554 intron variant C/A;G;T snv 0.94 1
rs11154370 6 126846446 intron variant A/G;T snv 1
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs1294410
LOC101928004
6 6738519 intron variant T/C snv 0.65 1
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs2894204
HLA-C
1.000 0.040 6 31269284 intron variant C/A;T snv 1