Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 7
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 4
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs1789924
ADH1C
0.925 0.160 4 99353129 upstream gene variant C/G;T snv 4
rs2094081
RHBDL2
0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs58598658
KLF12
0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs1154433
ADH1B
1.000 0.080 4 99332551 intron variant A/G;T snv 3
rs12898370
HMG20A
1.000 0.080 15 77516256 intergenic variant A/C;T snv 3
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs1437396 1.000 0.080 2 55278320 upstream gene variant C/G;T snv 3
rs1709817
KCNJ6
1.000 0.080 21 37664047 intron variant T/A;C snv 3
rs1709826
KCNJ6
1.000 0.080 21 37677171 intron variant G/A;C snv 3
rs1787395
KCNJ6
1.000 0.080 21 37664176 intron variant A/C;T snv 3
rs1787401
KCNJ6
1.000 0.080 21 37666591 intron variant C/G;T snv 3
rs1787402
KCNJ6
1.000 0.080 21 37666688 intron variant C/A;G;T snv 3
rs1787404
KCNJ6
1.000 0.080 21 37677060 intron variant A/C;G snv 3
rs2241894
ADH1C ; ADH1B
1.000 0.080 4 99344976 synonymous variant T/A;C snv 4.0E-06; 0.30 3
rs2835848
KCNJ6
1.000 0.080 21 37638771 intron variant C/G;T snv 3
rs2835898
KCNJ6 ; LOC107985507
1.000 0.080 21 37699478 intron variant T/A;C snv 3
rs3824435
PLGRKT
1.000 0.080 9 5377115 intron variant C/G;T snv 3
rs4715221 1.000 0.080 6 51495005 regulatory region variant G/A;C;T snv 3
rs4816568
KCNJ6
1.000 0.080 21 37616044 3 prime UTR variant A/G;T snv 3