Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 1
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
rs2820464
LYPLAL1-AS1
1 219519878 intergenic variant G/A;C snv 1
rs2894204
HLA-C
1.000 0.040 6 31269284 intron variant C/A;T snv 1
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs3088050
NSD1
5 177299634 3 prime UTR variant G/A snv 0.18 1
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs4640244
KCNJ12
17 21380911 intron variant A/G snv 0.33 1
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 1
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 1
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs55747707
MLXIPL
7 73623036 intron variant G/A snv 0.16 1
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs605203
EHMT2-AS1 ; LOC107986588 ; CYP21A2 ; SLC44A4
1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs620861
PCAT1 ; CASC8 ; POU5F1B ; CASC21
0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs634869 6 139510620 intron variant T/A;C snv 2
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1