Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10000770
INPP4B
1.000 0.040 4 142693109 intron variant C/T snv 0.11 1
rs10001414
PALLD
1.000 0.040 4 168569930 intron variant A/G snv 1.7E-02 1
rs10002854
SORCS2
1.000 0.040 4 7519419 intron variant C/T snv 8.8E-02 1
rs10004892 1.000 0.040 4 188951696 intergenic variant T/C snv 0.21 1
rs10006108 1.000 0.040 4 97002862 intergenic variant C/T snv 0.48 1
rs10006418
INPP4B
1.000 0.040 4 142691588 intron variant A/T snv 0.11 1
rs10010954
LRBA
1.000 0.040 4 150324302 intron variant T/A;C snv 1
rs10011263
ANK2
1.000 0.040 4 112807837 intergenic variant G/A snv 0.22 1
rs10012488
INPP4B
1.000 0.040 4 142671933 intron variant C/T snv 7.7E-02 1
rs10019259 1.000 0.040 4 95825984 intergenic variant C/A;T snv 1
rs10019567
LINC01378
1.000 0.040 4 117598351 intron variant T/C snv 0.23 1
rs10020323
NWD2
1.000 0.040 4 37448181 3 prime UTR variant G/A snv 0.23 1
rs10020457
PPARGC1A
1.000 0.040 4 23961338 intergenic variant G/A snv 0.31 1
rs10022002
PALLD
1.000 0.040 4 168563061 intron variant G/A snv 0.61 1
rs10025495
CFAP299
1.000 0.040 4 80618935 intron variant G/A;C;T snv 1
rs10027671 1.000 0.040 4 153056676 intron variant G/A snv 0.35 1
rs1002824
LNX1
1.000 0.040 4 53579813 intron variant C/A snv 0.27 1
rs10029800 1.000 0.040 4 152071589 intergenic variant C/A snv 0.63 1
rs10031537
FSTL5
1.000 0.040 4 162140692 intron variant T/C snv 0.53 1
rs10035359
TENM2
1.000 0.040 5 167575396 intron variant C/T snv 5.3E-02 1
rs10038027
AFF4
1.000 0.040 5 132895053 intron variant A/T snv 0.32 1
rs10038162
CTNNA1
1.000 0.040 5 138901066 intron variant G/A snv 0.31 1
rs10039512 1.000 0.040 5 68847366 intron variant C/G;T snv 1
rs1004000
GPHN
1.000 0.040 14 67430386 intergenic variant T/C snv 0.14 1
rs10040260 1.000 0.040 5 1749100 intergenic variant C/A;G snv 1