Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 2
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 1
rs876660634
PTEN
0.807 0.200 10 87925551 missense variant A/C;G snv 10
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 5
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
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 7
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs1276519904
H3-3A
0.645 0.520 1 226071445 missense variant A/G snv 63
rs369160589
ALG1
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04 35
rs80338945
GJB2
0.695 0.440 13 20189313 missense variant A/G snv 6.4E-04 6.4E-04 32
rs886041091
NTRK2
0.807 0.120 9 84751990 missense variant A/G snv 18
rs398122394
ALG13
0.763 0.240 X 111685040 missense variant A/G snv 16