Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2343506 1 162923134 intergenic variant A/C;T snv 1
rs2697963
PRDM2
1 13824245 3 prime UTR variant G/A;T snv 1
rs2809969 1 199832888 intergenic variant T/A;C snv 1
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 1
rs301803
RERE
1 8438620 intron variant A/T snv 0.30 1
rs320320
AKT3
1 243671884 intron variant A/G snv 0.30 1
rs35011283
FOXJ3
1 42300612 intron variant C/A;T snv 1
rs4133019 1 102042537 intergenic variant A/C;G;T snv 1
rs4360524 1 151127081 downstream gene variant A/G;T snv 1
rs4660257
KDM4A
1 43682497 intron variant T/C snv 0.23 1
rs466639
RXRG
1 165425645 intron variant T/A;C snv 1
rs4889
KISS1
0.882 0.160 1 204190659 missense variant G/A;C snv 5.2E-06; 0.29 1
rs506589
SEC16B
1 177925152 intron variant T/C snv 0.21 1
rs571567 1 177903770 intron variant G/A snv 0.17 1
rs61779781
LEPR
1 65468671 intron variant T/C snv 0.30 1
rs6427782 1 199829211 intergenic variant G/A snv 0.50 1
rs7514705
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1 74541036 intron variant T/C snv 0.41 1
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs17266097
SATB2
2 199410486 intron variant C/T snv 0.29 2
rs1861072
UNC80
2 209986910 intron variant T/C snv 0.34 2
rs2679894
TGFBRAP1
2 105254322 upstream gene variant A/G snv 0.43 2
rs10170108 2 136692386 intergenic variant G/A snv 0.53 1
rs11125803
ADCY3
2 24829308 intron variant C/T snv 0.68 1
rs112753638 2 202334496 upstream gene variant C/A;T snv 1
rs113467400
GREB1
2 11580173 intron variant C/T snv 0.11 1