Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113994198
PAFAH1B1
0.925 0.080 17 2666053 frameshift variant A/-;AA delins 4
rs1554208945
ZNF292
0.752 0.240 6 87260207 missense variant A/C snv 26
rs1064795104
EXOC6B
0.790 0.440 2 72498492 stop gained A/C snv 17
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11
rs1555103652
GRIN2B
0.882 0.240 12 13569973 missense variant A/C snv 11
rs1555570110
MPDU1
0.827 0.240 17 7586766 missense variant A/C snv 9
rs772887102
RARS2
0.807 0.200 6 87548623 missense variant A/C snv 2.2E-04 2.8E-05 9
rs869312822
GNB1
0.827 0.200 1 1806514 missense variant A/C snv 8
rs869312666
MTOR
0.925 0.160 1 11129789 missense variant A/C snv 4
rs1060499740
CINP
14 102348559 stop lost A/C snv 3
rs1461148946
FLNA
X 154354979 missense variant A/C snv 9.3E-06 3
rs121918751
SCN1A ; SCN1A-AS1 ; LOC102724058
1.000 0.040 2 165991841 missense variant A/C snv 2
rs1567230528
AP4E1
1.000 15 50949824 splice acceptor variant A/C snv 2
rs28937874
LGI1
1.000 0.120 10 93797277 missense variant A/C snv 2
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs876660634
PTEN
0.807 0.200 10 87925551 missense variant A/C;G snv 10
rs1404008939
ABCB1
0.925 0.200 7 87504324 missense variant A/C;G snv 4.0E-06 4
rs1064793923
SCN8A
12 51699581 missense variant A/C;G snv 1
rs752746786
GNB1
0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30
rs757511770
FMN2
0.807 0.280 1 240092656 missense variant A/C;G;T snv 8.0E-06; 4.0E-06 9
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1057524157
DEAF1
0.776 0.200 11 686962 missense variant A/C;T snv 19
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 8
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131