Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 7
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 1
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 1
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 2
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 1
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 18
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 10
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs1065852
NDUFA6-DT ; LOC112268294 ; CYP2D6
0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 2
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 17
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 1