Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555366607
SPTB
1.000 0.080 14 64767787 missense variant A/G snv 5
rs1555889984
RUNX1
0.925 0.120 21 34834536 stop gained C/A snv 5
rs4719714
STEAP1B
1.000 0.080 7 22721094 intron variant A/T snv 0.21 5
rs9332377
ARVCF ; COMT
0.882 0.120 22 19968169 intron variant C/A;T snv 5
rs1057518925
COL6A2
1.000 0.120 21 46114006 splice acceptor variant A/G snv 4
rs1553315329
SPAST
2 32116153 stop gained C/A;T snv 3
rs11214105
TEX12 ; LOC107987164
1.000 0.120 11 112166930 intron variant G/A snv 0.25 2
rs2293052
NOS1
1.000 0.040 12 117277815 intron variant G/A snv 0.28 2
rs3766246
FAAH
1 46399999 intron variant A/C;G snv 2
rs3783642
GCH1
14 54893485 intron variant T/A;C snv 2
rs9524885
ABCC4
13 95283335 intron variant T/C snv 0.63 2
rs17841327
SLC6A2
16 55660341 intron variant A/C snv 0.63 1
rs2287396
GSTZ1
14 77327849 non coding transcript exon variant C/T snv 0.15 1
rs574584
ADRA1A
8 26866167 intron variant C/G;T snv 1
rs949060 18 77246982 upstream gene variant C/A;G snv 1
rs9658498
NOS1
12 117230720 intron variant A/C;G snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3740071
ABCC2
10 99830363 missense variant G/A;C snv 4.0E-06; 4.0E-06 1
rs1042718
ADRB2
0.925 0.080 5 148827354 missense variant C/A;T snv 0.23; 4.0E-06 3
rs387907170
ETFDH
0.925 0.080 4 158703436 missense variant T/C snv 4.0E-06 3
rs756877019
MUSK
1.000 9 110800760 missense variant G/C snv 4.0E-06 3
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs199682734
OPRM1
6 154118718 synonymous variant C/T snv 8.1E-06 7.0E-06 1
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57