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
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 10
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs3738401
DISC1 ; TSNAX-DISC1
0.882 0.080 1 231694549 missense variant G/A snv 0.30 0.26 4
rs10494561
NMNAT2
1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 3
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs951436 0.925 0.040 1 163063552 regulatory region variant A/C snv 0.42 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
rs751229
DISC1 ; TSNAX-DISC1
1.000 0.040 1 231632793 intron variant A/G;T snv 2
rs1655285
TSNAX-DISC1 ; TSNAX
1 231563728 intron variant G/C snv 9.5E-02 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs934945
PER2
0.827 0.200 2 238246412 missense variant C/T snv 0.21 0.15 10
rs10496702
NCKAP5
2 133247997 intron variant G/A snv 0.18 2
rs12105421
TMEM182
1.000 0.040 2 102959630 intron variant C/T snv 7.8E-02 2
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 2
rs701492
GAD1
1.000 0.040 2 170845970 intron variant C/T snv 0.30 0.28 2
rs7600871
NCKAP5
2 133257389 intron variant C/T snv 0.16 2
rs769404
GAD1
1.000 0.040 2 170822115 synonymous variant T/C snv 0.39 0.35 2