Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12374521
LOC107986462 ; HTR4
5 148457317 intron variant C/T snv 0.45 2
rs1659127 16 14294448 intergenic variant G/A;C;T snv 2
rs314268
LIN28B
6 104970103 intron variant G/A snv 0.64 2
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 2
rs4549631 6 126645162 intron variant T/C;G snv 2
rs7846385 8 77247943 intergenic variant T/C snv 0.23 2
rs7861820
LINC01505
9 106174393 intron variant T/C snv 0.62 2
rs9391253
LIN28B-AS1
6 104919741 intron variant A/T snv 0.29 2
rs10007754
TACR3
4 103706285 intron variant T/G snv 0.34 1
rs10019555
TACR3
4 103694124 intron variant G/A;C snv 1
rs10156597
LINC01505
9 106179228 intron variant A/T snv 0.36 1
rs10423674
CRTC1
19 18707093 intron variant C/A;T snv 1
rs10441737
ZNF483
9 111539305 intron variant C/T snv 0.59 1
rs10453225
LINC01505
9 106157939 intron variant G/T snv 0.36 1
rs10899489
GAB2
11 78384327 non coding transcript exon variant C/A;T snv 1
rs10940138 5 67898641 intron variant C/T snv 0.21 1
rs10978430
LINC01505
9 106153728 intron variant C/T snv 0.33 1
rs10980926
ZNF483
9 111531354 intron variant A/G snv 0.56 1
rs12200251
LIN28B-AS1
6 104934540 intron variant G/A snv 0.46 1
rs12352703
LINC01505
9 106154985 intron variant G/T snv 0.32 1
rs12472911
LRP1B
2 141470940 intron variant C/A;T snv 1
rs12617311
LOC105373831
2 198767841 intron variant G/A snv 0.28 1
rs12686569
LINC01505
9 106154430 intron variant G/T snv 0.30 1
rs12907866
MIR4713HG ; CYP19A1
15 51253257 intron variant A/G snv 0.35 1
rs13187289 5 134513486 upstream gene variant C/A;G snv 0.19 1