Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036386
PDE8B
1.000 0.040 5 77247778 intron variant C/T snv 0.40 2
rs10180754
LINC01934
1.000 0.040 2 181238244 splice region variant G/A snv 0.35 1
rs10223666
LOC105375069 ; LOC107986598
1.000 0.040 6 43837765 intron variant G/A;C snv 3
rs10277273
FOXK1
1.000 0.040 7 4745498 intron variant T/C;G snv 1
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs10424978 0.851 0.080 19 4837545 upstream gene variant C/A;G snv 4
rs1047578
NAA25
1.000 0.040 12 112027325 3 prime UTR variant A/G;T snv 1
rs10489626
IL12RB2
1.000 0.040 1 67327488 intron variant C/G;T snv 0.17 1
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 4
rs1057516033
KAT6B
0.807 0.400 10 75025250 splice donor variant G/A snv 9
rs1057518799
POGZ
0.925 0.080 1 151430715 frameshift variant -/GATTGGCA delins 7
rs1057518891
CHD7
0.851 0.120 8 60854479 stop gained C/T snv 6
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13
rs1064191 1.000 0.040 6 31107598 downstream gene variant T/A;C snv 1
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10759927
PTCSC2
1.000 0.040 9 97779894 intron variant A/G snv 0.72 1
rs10759944
PTCSC2
0.925 0.080 9 97794690 intron variant A/G snv 0.72 4
rs10761620
LINC02621
1.000 0.040 10 62297443 intron variant A/G snv 0.53 1
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs1079418
PDE10A
1.000 0.040 6 165633546 intron variant A/G snv 0.32 1
rs10821973
LINC02621
1.000 0.040 10 62292578 intron variant G/A;C snv 1
rs1085308047
PTEN ; KLLN
0.827 0.160 10 87864509 missense variant A/G snv 6
rs10866828
SLC25A37
1.000 0.040 8 23544021 intron variant C/T snv 0.38 1
rs10917477
MICOS10
1.000 0.040 1 19534612 intron variant A/C;G;T snv 2
rs10930013
TANK
1.000 0.040 2 161213814 intron variant G/A snv 0.43 2