Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 3
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 4
rs9943291
HMGCS2
1 119749667 intron variant T/G snv 8.2E-02 3
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs272889
SLC22A4 ; MIR3936HG
5 132329685 intron variant A/G snv 0.64 2
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16