Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs16978075
LINC01478 ; LINC01601
18 44533186 intron variant T/C snv 8.5E-02 5
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 4
rs13212562 0.925 0.120 6 27332531 intergenic variant A/G snv 0.13 4
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs71636784
ZDHHC18
1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs7832708
MSRA
8 10332530 intron variant C/T snv 0.49 4
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42 4
rs10752262
CAMK1D
1.000 0.040 10 12353101 intron variant C/T snv 0.39 3
rs11765189
PTPRN2
1.000 0.040 7 157743285 intron variant A/G snv 0.25 3
rs12602286
EPN2
1.000 0.040 17 19333641 intron variant G/T snv 0.79 3
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs2093210
C14orf39
1.000 0.040 14 60490561 intron variant C/T snv 0.45 3
rs2629540
FAM53B
0.925 0.080 10 124737579 intron variant G/C snv 0.18 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs6119267
NOL4L-DT ; NOL4L
20 32576112 intron variant C/A;G snv 3
rs613872
TCF4
0.851 0.120 18 55543071 intron variant G/T snv 0.88 3
rs62154720
TGFBRAP1
1.000 0.040 2 105306623 intron variant C/T snv 9.2E-02 3
rs6731373
LOC107985892
2 68275912 intergenic variant G/A snv 0.29 3
rs6870983
TMEM161B-AS1
5 88401716 intron variant C/T snv 0.29 3
rs72829446
ATP1B2
17 7648805 intron variant C/T snv 6.5E-02 3
rs75757892
RREB1
6 7232156 intron variant C/T snv 0.12 3