Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs2228428
CCR4
0.925 0.120 3 32954436 synonymous variant C/T snv 0.25 0.23 2
rs17006471
CD207
1.000 0.120 2 70841493 intergenic variant T/C snv 0.42 1
rs77152992
CDKAL1
0.925 0.120 6 21065218 missense variant C/A;G;T snv 8.2E-06; 6.4E-02 2
rs2059876
CHST8
0.925 0.120 19 33639430 intron variant C/T snv 0.28 2
rs893051
CLDN1
0.807 0.400 3 190321812 intron variant G/A;C snv 7
rs9290929
CLDN16
0.925 0.120 3 190325950 intron variant G/A snv 0.65 2
rs2041733
CLEC16A ; LOC105371081
1.000 0.120 16 11135732 intron variant T/C;G snv 1
rs1800875
CMA1
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12
rs2248359
CYP24A1
0.790 0.400 20 54174979 upstream gene variant C/T snv 0.47 8
rs4674343
CYP27A1
1.000 0.120 2 218795623 intron variant A/G snv 0.48 1
rs320995
CYSLTR1
0.851 0.240 X 78272820 missense variant G/A;C;T snv 0.73 4
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs11362
DEFB1
0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs1799946
DEFB1
0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs5743409
DEFB1
0.925 0.120 8 6879098 intron variant C/A;G snv 2
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 4
rs26618
ERAP1
0.882 0.200 5 96795133 missense variant T/A;C;G snv 0.22 0.22 3
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs2143950
FAM177A1 ; PPP2R3C ; LOC101927178
1.000 0.120 14 35103151 intron variant C/T snv 0.17 1
rs2427837
FCER1A
0.851 0.160 1 159288755 upstream gene variant G/A snv 0.20 5
rs2251746
FCER1A
0.882 0.120 1 159302270 intron variant T/C snv 0.20 3
rs3126085
FLG-AS1
0.851 0.280 1 152328341 intron variant G/A snv 0.29 5
rs941934
FLG-AS1
0.851 0.200 1 152417976 intron variant T/A;C snv 5
rs11204971
FLG-AS1
0.925 0.120 1 152286602 intron variant A/G snv 0.15 2