Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048886
SDHAF4
1.000 0.080 6 70579486 missense variant A/G snv 0.18 0.22 1
rs10490072 1.000 0.080 2 60442796 upstream gene variant T/C snv 0.19 1
rs10494366
LOC105371475 ; NOS1AP
0.851 0.200 1 162115895 intron variant G/T snv 0.54 1
rs10507349
RNF6
1.000 0.080 13 26207391 intron variant G/A snv 0.19 1
rs10508438
CDC123
1.000 0.080 10 12202080 intron variant G/A snv 0.32 1
rs10510110
PLEKHA1
0.925 0.120 10 122432914 3 prime UTR variant T/C snv 0.56 2
rs10510536
UBE2E2
1.000 0.080 3 23228279 intron variant T/C snv 0.16 1
rs10510537
UBE2E2
1.000 0.080 3 23280429 intron variant C/A snv 2.7E-02 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 4
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 2
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 1
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 3
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 1
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 1
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10757282 1.000 0.080 9 22133985 intergenic variant T/C snv 0.38 1
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 4
rs10761745
JMJD1C
0.882 0.240 10 63341311 intron variant G/C snv 0.87 1
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6