Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs3749034
GAD1
0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs1541374 4 105127203 intergenic variant T/A;G snv 5
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs8049439
ATXN2L
0.925 0.120 16 28826194 intron variant T/C;G snv 0.38 5
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 4
rs12569232
LOC107985258
0.882 0.280 1 211379722 intron variant G/C;T snv 4
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs2456973
LOC105369781 ; IKZF4 ; LOC105369780
0.925 0.040 12 56023144 intron variant A/C;G snv 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs1349265
THRB
1.000 0.040 3 24117896 3 prime UTR variant A/C;G snv 3
rs1620977
NEGR1
1.000 0.040 1 72263459 intron variant A/G;T snv 3
rs1906252 0.925 0.120 6 98102413 intron variant C/A;T snv 3
rs2302190
MTMR4
17 58507147 missense variant T/A;C snv 0.24 3
rs268134
SPRED2
0.925 0.120 2 65381229 intron variant A/C;G;T snv 3
rs3027001
CADM3-AS1 ; CADM3
1.000 0.040 1 159199673 intron variant C/G;T snv 3
rs3747631
LOC105371692 ; LRRN2
1.000 0.040 1 204618441 missense variant G/A;C snv 4.0E-06; 0.20 3
rs3843954 1.000 0.040 13 57974377 intergenic variant G/A;C snv 3
rs4664442
SLC4A10
1.000 0.040 2 161971491 intron variant G/A;C snv 3
rs4702
FES ; FURIN
1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv 3
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv 3
rs72986630
ZNF823
1.000 0.040 19 11738921 5 prime UTR variant C/A;T snv 3
rs7924036
JMJD1C
10 63431885 intron variant G/A;T snv 3