Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs2228611
DNMT1
0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs1554603293
CHD7
0.752 0.320 8 60849154 missense variant G/A snv 17
rs16999593
DNMT1
0.742 0.240 19 10180505 missense variant T/C snv 2.4E-02 9.6E-03 14
rs528302390
PKD1L1
0.776 0.120 7 47831214 splice donor variant AC/- delins 3.7E-04 5.0E-04 9
rs121434422
CERS1 ; GDF1
0.882 0.120 19 18869035 stop gained G/A;C;T snv 3
rs61743125
PTCRA
0.882 0.080 6 42925677 missense variant G/A snv 2.0E-02 1.9E-02 3
rs772953044
ACOT7
0.925 0.120 1 6333503 missense variant T/C;G snv 4.0E-06; 4.0E-06 2
rs1424438515
F11
0.925 0.080 4 186274140 missense variant A/G;T snv 4.0E-06 2
rs1324026337
TGM2
0.925 0.120 20 38148038 missense variant T/C snv 4.0E-06 2
rs752163489
TMPRSS6
0.925 0.120 22 37096044 stop gained C/A;T snv 1.8E-04 2
rs16999358
DNMT1
1.000 0.080 19 10162679 synonymous variant G/A snv 6.2E-03 2.4E-03 1
rs2276598
DNMT3A
1.000 0.080 2 25246633 synonymous variant C/T snv 0.19 0.21 1
rs2276599
DNMT3A
1.000 0.080 2 25247044 splice region variant C/T snv 0.71 0.69 1