Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 3
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 2
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs10883371
LINC01475 ; NKX2-3
1.000 0.040 10 99532698 upstream gene variant C/A snv 0.54 1
rs10905718 1.000 0.040 10 6072893 upstream gene variant A/G snv 0.25 1
rs12369214
RIC8B
0.807 0.120 12 106804833 intron variant G/A snv 0.41 1
rs12479056
PUS10
1.000 0.040 2 60948177 synonymous variant T/C snv 0.56 0.62 1
rs13132245 1.000 0.040 4 122128437 intergenic variant A/G snv 0.11 1
rs13140464 0.925 0.040 4 122578590 regulatory region variant G/T snv 0.10 1
rs1452787
TCF4
0.827 0.160 18 55539976 intron variant A/G snv 0.24 1
rs17683107
GAS7
1.000 0.040 17 9921085 intron variant G/A snv 0.13 1
rs1788097
CD226
0.925 0.040 18 69876452 intron variant C/T snv 0.56 1
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 1
rs2844559 1.000 0.040 6 31372298 intron variant C/T snv 8.0E-02 1