Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9822953
LINC00886
3 156754282 intron variant C/G;T snv 2
rs11790360
LINC02692
9 136971795 non coding transcript exon variant T/C;G snv 1.5E-05; 0.49 2
rs930847
LRRK1
15 101018357 intron variant G/T snv 0.67 2
rs3931397
NR3C2
1.000 0.080 4 148158346 intron variant G/T snv 0.11 2
rs12913547
SMAD3
15 67175169 intron variant T/C;G snv 2
rs785422
TJP1
15 29881682 intron variant C/T snv 1.0E-01 2
rs6430585
UBXN4
1.000 0.040 2 135749357 intron variant A/C snv 0.74 2
rs1034200 13 22654552 intergenic variant C/A;T snv 1
rs11145951 9 136965812 upstream gene variant T/C snv 0.44 1
rs11763147 7 65861834 upstream gene variant A/G snv 0.50 1
rs12940030 17 14657699 intergenic variant T/C snv 0.45 1
rs2323457 17 14650873 intergenic variant C/A snv 0.44 1
rs2755238 13 40536133 intron variant T/C snv 7.9E-02 1
rs3118516 9 134547946 upstream gene variant G/A snv 0.29 1
rs3132306 9 134548366 upstream gene variant T/C snv 0.31 1
rs4792534 17 14661532 intergenic variant A/G snv 0.45 1
rs4838968 1 112817815 downstream gene variant G/C snv 8.6E-02 1
rs4843049 15 85331141 upstream gene variant G/A snv 0.16 1
rs7676985 4 54198406 intron variant G/A snv 0.22 1
rs7682912 4 54219453 intron variant T/C;G snv 1
rs908839 9 136962187 regulatory region variant C/G snv 0.43 1
rs9512928 13 27939164 intergenic variant T/C snv 0.17 1
rs2307121
ADAMTS6
5 65329685 intron variant C/T snv 0.27 1
rs386188
ADAMTS6
5 65463848 intron variant T/C snv 0.36 1
rs10163187
ADAMTS7P4
15 85327287 intron variant C/T snv 0.29 1