Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 5
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 5
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs4502156 1.000 0.080 15 62090956 intergenic variant T/C snv 0.55 4
rs7172432 0.925 0.080 15 62104190 intergenic variant A/G snv 0.51 4
rs742642
CDKAL1
1.000 0.080 6 20664850 intron variant G/A snv 0.21 3
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 3
rs933360
GRB10
7 50690548 intron variant C/T snv 0.60 2
rs1051006
MADD
11 47285034 missense variant G/A;C snv 0.26; 4.0E-06 2
rs10838687
MADD
11 47291341 intron variant T/G snv 0.31 2
rs1549318 15 70816808 intergenic variant C/T snv 0.55 1
rs3824420
KANK1
9 712766 missense variant G/A;C snv 3.8E-02; 1.2E-05 1
rs35233100
MADD
11 47285079 stop gained C/T snv 3.8E-02 3.9E-02 1
rs6930337
SASH1
6 148466870 intron variant C/G;T snv 1
rs4790333
SGSM2
17 2359409 intron variant C/A;T snv 0.44 1
rs61741902
SGSM2
17 2379485 missense variant G/A snv 1.0E-02 9.1E-03 1
rs9727115
SNX7
1 98711697 intron variant G/A snv 0.37 1
rs150781447
TBC1D30
12 64830440 missense variant C/T snv 5.4E-03 5.3E-03 1