Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1034207 6 127016554 intron variant C/A;G;T snv 0.94 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
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 1
rs2894204
HLA-C
1.000 0.040 6 31269284 intron variant C/A;T snv 1
rs987763
LOC105377989
6 126960402 intron variant C/A;T snv 1
rs9491696
RSPO3
6 127131494 intron variant C/G snv 0.45 1
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 2
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs12731740
MIR29B2CHG
1 207851475 intron variant C/T snv 9.1E-02 1
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs17213965
MYH11
16 15788110 intron variant C/T snv 0.24 1
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 1
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs6784615
NISCH
1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1
rs6931262
RREB1
6 7217284 non coding transcript exon variant C/T snv 0.10 1