Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs115510139
COL6A3
0.827 0.120 2 237331726 intron variant A/T snv 0.60 6
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs315919
IL1RN
0.851 0.120 2 113118636 intron variant T/G snv 0.55 5
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
rs11125529
ACYP2
0.882 0.280 2 54248729 intron variant C/A;T snv 3
rs7436
COL6A3
0.925 0.080 2 237324168 3 prime UTR variant T/A snv 0.10 3
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs752742313
PIK3CB
0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs568408
IL12A ; IL12A-AS1
0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22