Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7590720
PECR ; MREG
1.000 0.080 2 216033935 intron variant G/A snv 0.73 3
rs896543
LOC107986001
1.000 0.080 2 236600564 intergenic variant G/A snv 0.33 3
rs11558538
LOC107985948 ; HNMT
0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 1
rs1869324
THSD7B
1.000 0.080 2 137469872 intron variant G/A snv 7.9E-02 1
rs7607774 1.000 0.080 2 236520511 intergenic variant G/A snv 7.4E-02 1
rs2002594
FAM162A
1.000 0.080 3 122392714 intron variant A/G snv 0.59 3
rs2168784 1.000 0.080 3 164872151 intergenic variant C/T snv 0.24 3
rs6777876 1.000 0.080 3 11915124 upstream gene variant A/G snv 9.9E-02 3
rs11922615
SETD5
1.000 0.080 3 9416623 intron variant A/G snv 8.4E-02 1
rs12489456
SLC6A6
1.000 0.080 3 14459666 intron variant G/A;T snv 1
rs2727943 0.925 0.080 3 1856289 intergenic variant T/A;C snv 1
rs3773165
SLC6A6
1.000 0.080 3 14482762 intron variant G/A snv 0.20 1
rs4384980 1.000 0.080 3 182741281 upstream gene variant A/C snv 0.48 1
rs6443238
SETD5
1.000 0.080 3 9407371 intron variant C/T snv 8.4E-02 1
rs6778524
PLCL2
1.000 0.080 3 16814451 intron variant T/C snv 8.3E-02 1
rs9847462 1.000 0.080 3 164840807 intergenic variant A/G snv 0.14 1
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
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
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
rs1154433
ADH1B
1.000 0.080 4 99332551 intron variant A/G;T snv 3
rs115460205
FSTL5
1.000 0.080 4 161890417 intron variant C/T snv 4.7E-02 3
rs12639833
ADH1C ; ADH1B
1.000 0.080 4 99346215 intron variant C/T snv 0.31 3