Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 10
rs1938516
ERVMER61-1
0.925 0.120 1 187433789 intron variant T/A snv 5.7E-02 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs7597593
ZNF804A
0.827 0.160 2 184668853 intron variant T/C snv 0.53 6
rs2709370 0.851 0.120 2 207517878 intron variant A/C snv 0.17 4
rs6746896 0.851 0.120 2 96745212 intergenic variant A/G snv 0.26 4
rs6785
CREB1 ; METTL21A
0.851 0.120 2 207603273 3 prime UTR variant A/G snv 0.84 4
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs9836592
CHDH
0.925 0.120 3 53821056 intron variant C/T snv 0.74 2
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs28364997
SLC6A3
0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs187269
GABRB2
0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs2546620
GABRB2
0.882 0.120 5 161332120 intron variant T/C snv 0.15 3
rs41084
SGCD
0.925 0.120 5 156118554 intron variant A/T snv 0.45 2
rs6413429
SLC6A3
0.925 0.120 5 1446912 upstream gene variant C/A snv 6.1E-02 2
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs10947563
FKBP5
0.925 0.040 6 35685660 intron variant G/A snv 0.77 3
rs3798347
FKBP5 ; LOC112267956
0.925 0.040 6 35633999 intron variant A/T snv 0.65 3
rs1128306
HCG9 ; HLA-A
0.925 0.120 6 29975492 non coding transcript exon variant G/A snv 0.22 2
rs4713902
LOC112267956 ; FKBP5
1.000 0.040 6 35646249 intron variant T/C snv 0.21 1