Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 5
rs9291683 0.925 0.120 4 10322536 intergenic variant G/A;C;T snv 4
rs1047964
BACE1 ; RNF214
11 117286177 3 prime UTR variant G/A;C;T snv 3
rs10497870
NBEAL1
2 203105560 intron variant A/C;G snv 2
rs11720167 3 165768357 intron variant T/A;G snv 2
rs4975709
IRX4
5 1877166 downstream gene variant A/C;T snv 2
rs7698623
MEPE
4 87834676 intron variant T/A;C snv 6.1E-05; 0.94 2
rs1007845 3 165722308 intron variant C/A;G;T snv 1
rs10513622 3 166009461 intergenic variant G/A;C snv 1
rs10800805
LOC112268254 ; RNPEP
1 201990610 intron variant G/A;C snv 1
rs11586632
RNPEP
1 201986486 intron variant G/A;T snv 1
rs11679740
RAPH1
2 203450671 intron variant G/A;C snv 1
rs11683935
RAPH1
2 203513148 intron variant C/G;T snv 1
rs11686036
ABI2
2 203376916 intron variant A/G;T snv 1
rs11715356 3 166051370 intergenic variant C/A;G;T snv 1
rs1174605 2 203556781 intergenic variant T/A;C snv 1
rs11921875 3 165718131 intron variant A/C;G snv 1
rs11922912 3 166106549 intergenic variant T/A;C snv 1
rs11928507 3 166056006 intergenic variant G/C;T snv 1
rs12233613 3 166057646 intergenic variant T/A;C snv 1
rs12487357
BCHE
3 165804028 intron variant G/A;C snv 1
rs12638042 3 166191637 intergenic variant T/A;C snv 1
rs12696252 3 166580725 intergenic variant G/A;T snv 1
rs13061243 3 166141319 intergenic variant T/A;C snv 1