Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2303369
FNDC4
0.925 0.120 2 27492549 intron variant C/T snv 0.38 3
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3
rs1046089
PRRC2A
0.882 0.200 6 31635190 missense variant G/A snv 0.36 0.40 3
rs494620
SLC44A4 ; CYP21A2
0.925 0.120 6 31870936 stop gained G/A;T snv 0.44; 4.1E-06 3
rs7537437 1 38973866 regulatory region variant G/A snv 0.20 2
rs704795
FNDC4
0.925 0.120 2 27493627 intron variant G/A snv 0.46 2
rs7861820
LINC01505
9 106174393 intron variant T/C snv 0.62 2
rs10496265 2 81441684 intergenic variant T/C snv 0.12 1
rs10852344 16 11923062 upstream gene variant C/T snv 0.43 1
rs11195485 10 111244059 intergenic variant C/T snv 4.2E-03 1
rs11597068 10 123228637 intergenic variant A/G snv 0.11 1
rs117876865 21 34444399 downstream gene variant G/A snv 1
rs1473307 2 225360907 intergenic variant C/T snv 0.64 1
rs1528753 11 91151171 intergenic variant A/C snv 0.70 1
rs17153527 7 106855364 intergenic variant T/C snv 9.3E-02 1
rs2151145 9 79730966 downstream gene variant G/A snv 0.78 1
rs4397868 11 133697090 intergenic variant C/T snv 0.87 1
rs7333181 1.000 0.040 13 111568950 intergenic variant G/A snv 0.11 1
rs9635759 17 51536424 regulatory region variant G/A snv 0.25 1
rs6468442
ADGRA2
8 37829231 intron variant A/G snv 0.81 0.84 1
rs2517388
ASH2L
0.925 0.080 8 38120214 intron variant T/G snv 0.24 1
rs4843747
BANP
16 87957445 intron variant A/C snv 0.83 1
rs1551562
BRSK1
19 55303513 intron variant A/G snv 0.19 1
rs114158228
CDKAL1
6 20699892 intron variant T/A snv 4.2E-04 1
rs181686584
CERT1
5 75429983 intron variant C/T snv 6.7E-03 1