Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 4
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs4502156 1.000 0.080 15 62090956 intergenic variant T/C snv 0.55 3
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 3
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 2
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 2
rs1549318 15 70816808 intergenic variant C/T snv 0.55 1
rs7172432 0.925 0.080 15 62104190 intergenic variant A/G snv 0.51 1
rs742642
CDKAL1
1.000 0.080 6 20664850 intron variant G/A snv 0.21 1
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 1
rs1051006
MADD
11 47285034 missense variant G/A;C snv 0.26; 4.0E-06 1
rs10838687
MADD
11 47291341 intron variant T/G snv 0.31 1
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 1
rs4790333
SGSM2
17 2359409 intron variant C/A;T snv 0.44 1
rs9727115
SNX7
1 98711697 intron variant G/A snv 0.37 1