Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12098904 11 55899077 downstream gene variant A/T snv 5.7E-02 1
rs12098941 11 55898967 downstream gene variant T/A;G snv 1
rs12195036
LOC105378117
6 166038209 intergenic variant T/C snv 4.1E-02 2
rs12195230
KLHL32
6 97052171 intron variant G/C snv 0.23 2
rs1223397
PHACTR1 ; TBC1D7 ; TBC1D7-LOC100130357
6 13270713 intron variant G/A;C snv 0.19 2
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 5
rs12279202
IPO7
11 9410543 intron variant C/T snv 4.8E-02 2
rs12416687
BORCS7-ASMT ; AS3MT
10 102869254 intron variant T/C snv 0.21 2
rs12627514 1.000 0.040 21 43339560 intergenic variant C/A;G;T snv 3
rs12759054
SLC35F3
1.000 0.040 1 233984064 intron variant T/A;C snv 3
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 5
rs13002573 2 164058698 intron variant A/G snv 0.20 3
rs13040716 1.000 0.040 20 32182402 downstream gene variant A/G snv 1.0E-01 2
rs13082711 3 27496418 intergenic variant T/C snv 0.16 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs13306560
CLCN6 ; MTHFR
1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02 3
rs13424629
RRM2
2 10156359 intron variant T/C snv 0.15 1
rs1343040
MECOM ; MECOM-AS1
3 169468505 intron variant G/A snv 0.36 1
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1384089 11 56081540 upstream gene variant G/C snv 6.0E-02 1