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
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs4665965
MPV17
0.925 0.120 2 27313513 intron variant T/A;C snv 4
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 4
rs1783598
FCHSD2
1.000 0.080 11 73140418 intron variant C/G;T snv 3
rs10278336
YKT6
7 44205764 intron variant A/C;G snv 2
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs11195502 10 111279909 intergenic variant C/A;G;T snv 2
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2
rs2302593
SNRPD2 ; QPCTL
19 45693376 intron variant C/A;G snv 1.0E-04; 0.48 2
rs3816725
MADD
11 47284118 intron variant T/C;G snv 2
rs4237150
GLIS3
9 4290085 intron variant G/A;C;T snv 2
rs6113722
LINC00261
20 22576461 intron variant G/A;T snv 2
rs17712208
PROX1-AS1
1 213977102 intron variant T/A snv 2.1E-02 2
rs3138708
SLC2A2
3 171009914 intron variant T/G snv 3.1E-02 2
rs118137427 10 111217250 intergenic variant A/G snv 3.3E-02 2
rs11891554
PPM1G
2 27390750 intron variant G/A;T snv 7.1E-02 2
rs7101470
C11orf49
11 47032897 intron variant A/G snv 7.4E-02 2