Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 3
rs16938437
PHF21A
11 46031024 intron variant C/T snv 0.13 1
rs1862471
OLFM2
19 9889646 intron variant C/G snv 0.38 1
rs2798224
MSANTD1
1.000 0.120 4 3265941 intron variant G/A snv 0.45 1
rs12907866
MIR4713HG ; CYP19A1
15 51253257 intron variant A/G snv 0.35 1
rs1040070
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74512186 intron variant G/A;C snv 1
rs12472911
LRP1B
2 141470940 intron variant C/A;T snv 1
rs12374521
LOC107986462 ; HTR4
5 148457317 intron variant C/T snv 0.45 2
rs6438424
LOC107986022
3 117855975 intron variant A/C;T snv 1
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 2
rs12617311
LOC105373831
2 198767841 intron variant G/A snv 0.28 1
rs852069
LOC105372544
20 17141948 intergenic variant A/G snv 0.57 1
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 1
rs7662107
LINC02428
4 103337239 intron variant C/T snv 0.26 1
rs241036
LINC02210 ; LINC02210-CRHR1
17 45654353 non coding transcript exon variant A/C snv 0.14 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs17188434
LINC01876
2 156240264 intron variant T/C snv 4.4E-02 1
rs7861820
LINC01505
9 106174393 intron variant T/C snv 0.62 2
rs10156597
LINC01505
9 106179228 intron variant A/T snv 0.36 1
rs10453225
LINC01505
9 106157939 intron variant G/T snv 0.36 1
rs10978430
LINC01505
9 106153728 intron variant C/T snv 0.33 1
rs12352703
LINC01505
9 106154985 intron variant G/T snv 0.32 1
rs12686569
LINC01505
9 106154430 intron variant G/T snv 0.30 1
rs1516881
LINC01505
9 106150773 intron variant C/G;T snv 1