Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs756952113
EPHA4
1.000 0.120 2 221482561 missense variant C/T snv 4.0E-06 1
rs1258767
FMN1
1.000 0.120 15 32834253 intron variant A/G snv 0.18 1
rs180940944
NBEA
1.000 0.120 13 35375956 intron variant C/T snv 2.1E-02 1
rs12216499
RSPH3
1.000 0.120 6 158947492 intergenic variant G/T snv 0.11 1
rs397517792
TTN ; TTN-AS1
1.000 0.120 2 178764802 missense variant G/A snv 8.0E-06 2.8E-05 1
rs1937920 0.925 0.120 10 5119763 downstream gene variant A/G snv 0.28 2
rs4510656
CDKAL1
0.925 0.120 6 20766466 intron variant C/A snv 0.39 2
rs7747724
CDKAL1
0.925 0.120 6 20751084 intron variant T/C snv 0.41 2
rs150799650
CYP1B1 ; CYP1B1-AS1
0.925 0.120 2 38073618 non coding transcript exon variant G/T snv 7.0E-05 2
rs121913480
FGFR3
1.000 0.120 4 1806604 missense variant G/T snv 2
rs2836007
KCNJ6
0.925 0.120 21 37834589 intron variant C/T snv 0.21 2
rs6104690
LINC02871
0.925 0.120 20 11007451 intron variant G/A;T snv 2
rs5003154
PAG1
0.925 0.120 8 81074718 intron variant T/C;G snv 2
rs7238033
SLC14A1 ; LOC105372093
0.925 0.120 18 45737001 intron variant T/C snv 0.61 2
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 3
rs10234749 0.882 0.120 7 152690784 regulatory region variant T/C;G snv 3
rs62185668 0.925 0.120 20 10981287 intron variant C/A snv 0.19 3
rs6464268 0.882 0.120 7 152684065 intergenic variant A/G snv 0.23 3
rs715021 0.882 0.120 2 221196620 intergenic variant C/G snv 0.26 3
rs8102137 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 3
rs921142 0.882 0.120 8 41311757 upstream gene variant T/C snv 0.31 3
rs4986826
AHR
0.882 0.120 7 17339533 missense variant G/A snv 7.8E-03 2.2E-02 3
rs8041357
ARID3B
0.882 0.120 15 74577097 intron variant T/C snv 6.6E-02 3
rs11191438
AS3MT ; BORCS7-ASMT
0.882 0.120 10 102878107 intron variant G/A;C snv 3
rs7257330
CCNE1
0.882 0.120 19 29810916 upstream gene variant G/A snv 0.30 3