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
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs5177
LRP8
0.851 0.120 1 53246063 3 prime UTR variant G/A;C snv 6
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs11164835
DIPK1A
1 92913536 intron variant G/A snv 0.35 2
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 2
rs771065515
LMNA
1 156115240 missense variant A/G snv 2.5E-05 7.0E-06 2
rs144851946
LMNA
1 156138701 missense variant G/A;T snv 1.4E-04; 4.0E-06 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
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs121918805
LOC102724058 ; SCN1A-AS1 ; SCN1A
0.925 0.080 2 166002660 missense variant C/A;T snv 2.0E-05 4
rs4675690 2 207643083 intergenic variant C/T snv 0.48 3
rs10496702
NCKAP5
2 133247997 intron variant G/A snv 0.18 2
rs7600871
NCKAP5
2 133257389 intron variant C/T snv 0.16 2
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
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