Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10184428 2 164155317 intron variant C/A;G snv 5
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv 5
rs592373
LSP1
0.925 0.080 11 1869760 intron variant G/A;T snv 0.63; 6.8E-06 5
rs73036519
EXOC3L2 ; MARK4
0.851 0.040 19 45245104 intron variant G/A;C snv 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs1689040 12 89584456 intron variant C/G;T snv 4
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs2586886
KCNK3
1.000 0.080 2 26709163 intron variant C/G;T snv 4
rs2606736
ATG7
1.000 0.120 3 11358775 intron variant C/A;T snv 4
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs4712656
CASC15 ; NBAT1
1.000 0.040 6 22136033 non coding transcript exon variant G/A;C snv 4
rs4759319
HOXC4 ; HOXC6 ; HOXC5
12 54030947 intron variant G/C;T snv 4
rs4968782 1.000 0.080 17 63471115 upstream gene variant G/A;T snv 4
rs5762862
ZNRF3
22 28856744 intergenic variant G/A;T snv 4
rs62524579 8 142979538 downstream gene variant G/A;C;T snv 4
rs640065
NEK10
3 27322446 intron variant T/A;C snv 4
rs6418
GML ; CYP11B2
8 142914947 intron variant A/C;G snv 0.42 4
rs6969780
HOXA-AS2 ; HOXA3
7 27119517 splice region variant G/A;C snv 4