Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 3
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 3
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 3
rs1913641 0.925 0.120 8 75571004 downstream gene variant T/G snv 0.58 2
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 1
rs17536527 15 45426989 upstream gene variant G/A;C snv 1
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 1
rs227731 0.882 0.120 17 56695877 intergenic variant T/A;G snv 1
rs2453533 1.000 0.080 15 45349027 intergenic variant C/A snv 0.56 1
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 1
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 1
rs4441471 1.000 0.080 2 16534140 intron variant A/G snv 0.41 1
rs4886425 1.000 0.040 15 73832202 intergenic variant A/G snv 0.71 1
rs6465825 1.000 0.080 7 77787122 downstream gene variant T/C snv 0.41 1
rs807624 1.000 0.160 2 15642347 regulatory region variant G/T snv 0.47 1
rs10821905
A1CF
0.925 0.120 10 50886333 upstream gene variant G/A;T snv 2
rs10994856
A1CF
0.925 0.120 10 50885488 intron variant G/A snv 0.19 2
rs10994860
A1CF
0.925 0.120 10 50885664 5 prime UTR variant C/T snv 0.19 2
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 1
rs10206899
ALMS1P1
2 73673773 intron variant T/C;G snv 0.21; 3.9E-05 2
rs10821944
ARID5B
1.000 0.120 10 62025330 3 prime UTR variant G/T snv 0.66 1
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 3