Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77692382 1 39941043 downstream gene variant C/T snv 0.16 3
rs861409
SPTA1
1 158650687 intron variant C/A;G snv 3
rs1043897
GALNT2
1 230280653 3 prime UTR variant G/T snv 0.49 2
rs10801851
HFM1
1 91281449 intron variant C/T snv 0.48 2
rs10900586
ATP2B4
1 203684957 intron variant G/A snv 0.83 2
rs10923398 1 117708553 regulatory region variant A/C snv 0.16 2
rs10926973
CEP170
1 243225068 intron variant A/T snv 0.39 2
rs11119784
LINC01693
1 211641622 intron variant C/A;T snv 2
rs11122449
GALNT2
1 230164735 intron variant C/G;T snv 0.56 2
rs11265038
SPTA1
1 158626052 intron variant C/A snv 0.27 2
rs1166708
MIGA1
1 77865541 intron variant C/G;T snv 2
rs11799474 1 22377698 intergenic variant T/G snv 0.20 2
rs12038888 1 212192711 downstream gene variant A/T snv 0.32 2
rs12097784
LOC105371460
1 158163271 intergenic variant C/G snv 0.15 2
rs12137294 1 205213744 upstream gene variant A/C snv 0.46 2
rs12406643
ZNF691
1 42845892 intron variant A/G snv 0.16 2
rs12411257
LOC105378740
1 55817659 intron variant C/T snv 0.42 2
rs12724449
HCN3
1 155286440 intron variant A/C;T snv 2
rs12730156
ST7L
1 112587437 intron variant A/G snv 0.12 2
rs12739181
PLEKHG5
1 6518471 intron variant A/G;T snv 2
rs12760654 1 47203653 intergenic variant G/A snv 0.17 2
rs1355642
PIK3R3 ; P3R3URF-PIK3R3 ; LOC101929626
1 46133231 intron variant A/G snv 0.47 2
rs143670081
RSRP1 ; RHD
1 25295753 intron variant A/G snv 5.7E-02 2
rs1546954
GALNT2
1 230168102 intron variant T/G snv 0.46 2
rs17564336 1 151376698 upstream gene variant G/T snv 0.24 2