Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3792192
PLA2R1
0.925 0.160 2 160030364 intron variant G/A snv 0.35 2
rs601162 0.925 0.160 9 29632144 upstream gene variant A/C;G;T snv 2
rs6697139 0.925 0.160 1 161690906 intergenic variant G/A;T snv 2
rs7692514 0.925 0.160 4 65276878 intergenic variant G/A;C snv 2
rs7773456 0.925 0.160 6 19823007 intron variant T/G snv 0.35 2
rs7834765
LOC107986971
0.925 0.160 8 121263666 regulatory region variant G/T snv 0.32 2
rs8012283
NIN
0.925 0.160 14 50767442 intron variant A/G snv 0.23 2
rs958476
LOC107984410 ; BARX2
0.925 0.160 11 129451923 3 prime UTR variant T/A;G snv 2
rs8091180
NFATC1
1.000 0.160 18 79404243 intron variant G/A snv 0.46 3
rs114580964
PRRC2A
1.000 0.160 6 31636736 missense variant C/A;T snv 3.4E-03 1.4E-03 1
rs17008504 1.000 0.160 4 124718662 intergenic variant T/A snv 4.3E-02 1
rs2157257
MYH9
1.000 0.160 22 36312293 intron variant A/G snv 0.52 1
rs2271100
AGA
1.000 0.160 4 177438525 intron variant T/C snv 0.19 1
rs6056923
PAK5
1.000 0.160 20 9840271 intron variant T/C snv 0.10 1