Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3181052
IL1RN
0.851 0.120 2 113128472 intron variant G/A snv 0.16 5
rs1595066
ERBB4
0.882 0.080 2 211377000 3 prime UTR variant C/T snv 0.28 4
rs16845990
ERBB4
0.882 0.080 2 211378286 3 prime UTR variant T/A;C snv 4
rs2244438
TRAK2
0.882 0.080 2 201387816 missense variant G/A;T snv 0.29; 4.0E-06 4
rs3738894
PRKCE
0.882 0.080 2 46187030 3 prime UTR variant G/A snv 1.1E-02 4
rs6720283
COL6A3
0.882 0.120 2 237401239 intron variant G/A snv 0.31 4
rs7436
COL6A3
0.925 0.080 2 237324168 3 prime UTR variant T/A snv 0.10 3
rs17028375 1.000 0.080 2 64085008 downstream gene variant T/C snv 0.11 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs752742313
PIK3CB
0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs568408
IL12A ; IL12A-AS1
0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs2243115
IL12A-AS1 ; IL12A
0.776 0.320 3 159988493 intron variant T/G snv 0.10 12
rs767551092
XPC
0.790 0.200 3 14164838 missense variant G/A snv 4.0E-06 10
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 7
rs104893819
TGFBR2
0.827 0.240 3 30688470 stop gained C/G;T snv 5
rs6772209 1.000 0.080 3 175929377 intergenic variant G/A snv 4.1E-02 2
rs9868873
SEMA5B
1.000 0.080 3 123012063 intron variant G/A snv 0.28 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs989902
PTPN13
0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs353163
UBA6-AS1 ; TMPRSS11A
0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67 4
rs1014867
FAT4
0.925 0.080 4 125491736 missense variant C/T snv 4.9E-02 4.9E-02 3
rs1039808
FAT4
0.925 0.080 4 125318831 missense variant C/G;T snv 4.0E-06; 0.41 3