Source: GWASCAT ×
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 24
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs1541374 4 105127203 intergenic variant T/A;G snv 3
rs1620977
NEGR1
1.000 0.040 1 72263459 intron variant A/G;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
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
rs8049439
ATXN2L
0.925 0.120 16 28826194 intron variant T/C;G snv 0.38 3
rs9556958
FARP1 ; STK24
1.000 0.040 13 98447792 3 prime UTR variant C/G;T snv 3
rs9636107
TCF4
1.000 0.040 18 55532886 intron variant A/G;T snv 3
rs9906944
IGF2BP1
17 49014058 intron variant C/G;T snv 3
rs10061788
LINC00461
1.000 0.040 5 88638889 intron variant G/A;T snv 2
rs10757417 1.000 0.040 9 23347855 intron variant G/A;T snv 2
rs1076884 1.000 0.040 16 13653946 intergenic variant C/G;T snv 2