Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4699052 0.925 0.200 4 103216633 intergenic variant C/T snv 0.44 2
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 1
rs17483466
MIR4435-2HG ; ACOXL
0.827 0.280 2 111039881 intron variant A/G snv 0.15 3
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 2
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs2089222
MAP1LC3B2
0.925 0.200 12 116564853 intron variant G/A snv 0.12 2
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 2
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 2
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 2
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 2
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 2
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 2
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 4
rs4962416
CTBP2
0.882 0.160 10 125008303 intron variant T/C snv 0.23 2
rs1016343
PCAT2 ; PCAT1 ; PRNCR1 ; CASC19
0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 2
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 2
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 2
rs2180341
RNF146
0.882 0.160 6 127279485 intron variant G/A snv 0.73 2
rs16902094
CASC21 ; PCAT1 ; CASC8
0.882 0.160 8 127308101 intron variant A/G snv 0.15 2
rs445114
CASC21 ; PCAT1 ; CASC8
0.882 0.160 8 127310936 intron variant T/A;C snv 2
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 2
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 3
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 3