Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs504615 6 44627475 regulatory region variant G/A snv 0.78 1
rs556512 6 44626455 intergenic variant A/G snv 0.69 1
rs55825297 12 19017419 intergenic variant G/A snv 3.6E-02 1
rs56031230 12 19018473 regulatory region variant T/G snv 3.6E-02 1
rs7156510 14 84136819 intron variant G/T snv 0.64 1
rs7283054 21 30146989 intergenic variant G/C snv 1.3E-02 1
rs731991 22 30629202 downstream gene variant A/G;T snv 1
rs75188332 8 132863908 upstream gene variant T/G snv 6.6E-02 1
rs9345396 6 93779501 regulatory region variant C/T snv 1.7E-02 1
rs9472313 6 44624969 regulatory region variant G/A snv 0.26 1
rs9604365 13 111922883 intergenic variant G/A snv 0.82 1
rs1480544
AADAT ; LOC107986326
4 170066485 splice region variant A/G;T snv 0.57; 4.0E-04 1
rs2283436
ABHD2
15 89188545 intron variant T/C snv 9.6E-02 1
rs28793911
ADAMTS13
9 133434817 intron variant T/C;G snv 1
rs773162136
ALOX5
10 45443060 missense variant G/A snv 4.0E-06 1
rs3803277
ALOX5AP
13 30744171 non coding transcript exon variant C/A snv 0.49 0.45 1
rs4769060
ALOX5AP
13 30763740 intron variant A/G snv 0.35 1
rs398098426
ANKS1B
12 99246167 intron variant TT/-;T;TTT delins 0.20 1
rs1986743
ARL6IP6
2 152730385 intron variant A/G;T snv 1
rs13407662
ASB3
2 53555422 intron variant C/T snv 4.4E-02 1
rs215976
CACNA1C
12 2585472 missense variant C/G;T snv 0.11 1
rs10848683
CACNA1C-AS1 ; CACNA1C
12 2681964 missense variant C/T snv 4.0E-06; 0.78 0.71 1
rs574603859
CALCRL ; LOC105373786
2 187436817 intron variant A/T snv 1
rs9467504
CARMIL1 ; CMAHP
6 25414097 intron variant A/G snv 0.18 1
rs309247
CCDC102B ; TMX3
18 68715827 intron variant C/G snv 7.3E-02 1