Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912439
SOD1
0.851 0.080 21 31667320 missense variant A/G snv 4
rs121912445
SOD1
0.882 0.080 21 31667331 missense variant A/T snv 4
rs12891047
ZFYVE26
0.851 0.080 14 67776358 intron variant C/A snv 0.62 4
rs13100616
KCNMB2-AS1 ; KCNMB2
0.851 0.080 3 178681763 intron variant A/G snv 0.33 4
rs1400816
SLC25A12
0.851 0.080 2 171824168 intron variant A/C snv 0.81 4
rs1464443
ERBB4
0.851 0.080 2 212050001 intron variant C/A;T snv 4
rs1559473 0.851 0.080 2 222016799 intergenic variant T/G snv 0.25 4
rs1605070 0.851 0.080 3 51882999 intergenic variant C/A snv 0.60 4
rs16938145 0.851 0.080 9 2256092 intergenic variant T/C;G snv 4
rs16975050 0.851 0.080 18 41607206 intron variant T/G snv 7.0E-02 4
rs17162257 0.851 0.080 1 26602511 upstream gene variant T/A;G snv 4
rs2322978 0.851 0.080 11 127846245 intergenic variant A/G snv 0.74 4
rs2457174
FSTL4
0.851 0.080 5 133843389 intergenic variant C/T snv 0.33 4
rs2667100
INPP4B
0.851 0.080 4 142054920 intron variant A/G snv 0.81 4
rs2685056
LOC107986108
0.851 0.080 3 104699729 intergenic variant G/A snv 0.50 4
rs3852053
MASP1
0.851 0.080 3 187219412 3 prime UTR variant T/G snv 0.47 4
rs4148112
ABCG1
0.851 0.080 21 42230666 intron variant C/T snv 1.8E-03 4
rs4424056 0.851 0.080 6 91135689 intergenic variant T/G snv 0.76 4
rs4482178
LINC00351
0.851 0.080 13 85529954 intron variant C/A snv 8.4E-02 4
rs4761659
LOC643339
0.851 0.080 12 93293308 regulatory region variant T/C snv 0.89 4
rs551585 0.851 0.080 1 76660688 intergenic variant C/A snv 8.9E-02 4
rs6137726 0.851 0.080 20 22691782 intron variant C/A snv 0.25 4
rs7117082
OPCML
0.851 0.080 11 133522399 intron variant G/T snv 0.22 4
rs7148498 0.851 0.080 14 95641618 intron variant C/T snv 0.12 4
rs72911847 0.851 0.080 2 193714051 intergenic variant A/G snv 3.3E-02 4