Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4813376
RIN2
20 19870811 intron variant T/G snv 0.86 2
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs6024905
BPI
20 38329435 intron variant G/A snv 0.47 2
rs6046396
RIN2
20 19871859 non coding transcript exon variant G/A snv 0.68 2
rs6444931
CLDN11
3 170445686 intron variant G/A snv 0.85 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs7065696
PHF8
X 53947621 intron variant C/G;T snv 2
rs7248363
PGPEP1
19 18357076 intron variant T/C snv 0.74 2
rs7600871
NCKAP5
2 133257389 intron variant C/T snv 0.16 2
rs771065515
LMNA
1 156115240 missense variant A/G snv 2.5E-05 7.0E-06 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs993804
RARB
3 25070680 intron variant C/T snv 0.75 2
rs144851946
LMNA
1 156138701 missense variant G/A;T snv 1.4E-04; 4.0E-06 1
rs2020933
SLC6A4
17 30234737 intron variant A/T snv 0.14 1
rs373584456
LMNA
1 156136335 missense variant C/T snv 2.4E-05 2.1E-05 1
rs374726751
LMNA
1 156136245 missense variant C/T snv 2.4E-05 3.5E-05 1
rs374926367
LMNA
1 156139089 missense variant A/G snv 1.2E-04 1.0E-04 1
rs59190448
OXTR ; CAV3
3 8761315 intron variant G/A snv 0.12 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169