Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7217270
TRPV3
1.000 0.040 17 3518181 intron variant A/C;G snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs6557170
ESR1
1.000 0.040 6 151881969 intron variant A/G snv 0.79 1
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs6478241
ASTN2
0.925 0.040 9 116490350 intron variant A/G;T snv 3
rs2860174
INSR
1.000 0.040 19 7130707 intron variant A/T snv 0.18 1
rs12134493 0.925 0.040 1 115135325 TF binding site variant C/A snv 9.2E-02 4
rs2274316
MEF2D
0.925 0.040 1 156476450 intron variant C/A snv 0.62 0.54 3
rs2820651
ADARB2
1.000 0.040 10 1429570 intron variant C/A snv 0.14 2
rs1202430946
IGHMBP2
0.827 0.080 11 68930251 non coding transcript exon variant C/A;T snv 1.4E-05 17
rs1568523935
SLC25A42
0.776 0.240 19 19105656 stop gained C/G snv 20
rs7015657 1.000 0.040 8 21110040 intron variant C/G snv 0.30 2
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6790925
LOC101927995 ; LOC105377013
0.925 0.040 3 30438593 intergenic variant C/G;T snv 3
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs121908211
CACNA1A
0.882 0.080 19 13371744 missense variant C/T snv 5
rs10504861
LOC105375630 ; LOC105375629
0.925 0.040 8 88535703 intron variant C/T snv 0.23 3
rs4379368
SUGCT
0.925 0.040 7 40426601 intron variant C/T snv 0.12 3
rs12454023
NEDD4L
1.000 0.040 18 58342372 intron variant C/T snv 0.47 2
rs2986961 1.000 0.040 10 29798430 regulatory region variant C/T snv 0.65 2
rs41276886
CACNA1A
0.925 0.080 19 13317310 missense variant C/T snv 4.5E-03 4.4E-03 2