Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 3
rs10278336
YKT6
7 44205764 intron variant A/C;G snv 2
rs10500292
SYMPK
19 45824675 intron variant C/T snv 0.46 2
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 7
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 4
rs11039119
MIR6745 ; PACSIN3
11 47180373 intron variant G/A snv 0.38 0.33 2
rs11039130 11 47207765 intergenic variant C/T snv 0.20 2
rs11039182
MADD
11 47325172 intron variant T/C snv 0.19 2
rs11195502 10 111279909 intergenic variant C/A;G;T snv 2
rs1124649
TMEM214
2 27037601 missense variant G/A snv 0.32 0.35 2
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 5
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 5
rs11607883 11 45818158 intron variant G/A snv 0.40 2
rs11619319
PLUT
13 27913462 intron variant A/G snv 0.23 2
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 5
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2