Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs104895321
MVK
0.882 0.240 12 109591301 missense variant C/G;T snv 1.4E-04 4
rs104895358
MVK
12 109595148 missense variant G/A snv 1.2E-05 2
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1057518011
TMEM240
1 1535766 missense variant C/T snv 4
rs1057518644
HGSNAT
0.925 0.120 8 43192413 stop gained C/T snv 10
rs1057519475
FOXC1
1.000 0.080 6 1610761 stop gained C/T snv 2
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs1060504185
CDKN2A
9 21971116 missense variant G/A;C snv 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1156401234
YARS2 ; DNM1L
12 32740421 missense variant G/A snv 4.0E-06 1
rs1170695
SLC6A1 ; SLC6A1-AS1
1.000 0.040 3 11013652 5 prime UTR variant A/G snv 0.35 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908153
NLRP3
0.882 0.080 1 247424356 missense variant G/A;C snv 4
rs121908672
LRP5
0.925 0.080 11 68357802 missense variant C/T snv 3
rs121909731
GLUD1
0.851 0.120 10 87057692 missense variant G/A;C snv 4.0E-06 7
rs121912436
SOD1
0.827 0.080 21 31667274 missense variant G/A;C snv 7
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121912678
ACVR1
0.851 0.080 2 157774114 missense variant C/G;T snv 8
rs121912703
ACE
17 63496977 missense variant C/T snv 3.7E-05 4.9E-05 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 13