Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs221798
GIGYF1
0.882 0.040 7 100689872 intron variant C/A;G snv 3
rs4148087
ABCG1
1.000 0.040 21 42202157 intron variant G/A;T snv 3
rs6558872
CSMD1
0.882 0.040 8 4380617 intron variant G/A;C snv 3
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs7766730 0.882 0.040 6 65987110 intergenic variant C/A;T snv 3
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs9378249 0.925 0.160 6 31359924 upstream gene variant T/A;G snv 3
rs10058613
KDM3B
0.925 0.040 5 138358306 intron variant C/A;G;T snv 2
rs10457441 1.000 0.040 6 98124244 intron variant T/A;C snv 2
rs10865974
PBRM1 ; GNL3
0.925 0.040 3 52684264 intron variant G/C;T snv 2
rs111940429
LINC01789
0.925 0.080 2 107366232 intron variant C/A;T snv 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 2
rs12487445
PBRM1
0.925 0.040 3 52584303 intron variant A/C;T snv 2
rs12635140
SPCS1 ; GLT8D1
0.925 0.040 3 52704149 intron variant T/A;C snv 2
rs13068293
PBRM1
0.925 0.040 3 52638151 intron variant C/A;G snv 2
rs142425863 0.925 0.040 6 29783976 intergenic variant C/T snv 2
rs144373461 0.925 0.040 6 29783228 intergenic variant C/A snv 2
rs17541406
LOC105370982
1.000 0.040 15 93346230 intron variant C/A;G;T snv 2
rs2336146
PBRM1
0.925 0.040 3 52592630 intron variant A/G;T snv 2
rs2336149
PBRM1
0.925 0.040 3 52658108 intron variant G/A;C snv 2
rs2875907
CADM2
0.925 0.040 3 85469430 intron variant A/G;T snv 2
rs290475
TCF7L2
1.000 0.040 10 113114260 intron variant C/A;T snv 2
rs300774 0.925 0.040 2 112496 intergenic variant A/C;T snv 2
rs3733045
PBRM1
0.925 0.040 3 52609291 non coding transcript exon variant A/G;T snv 0.44 2
rs3755798
GLT8D1 ; SPCS1
0.925 0.040 3 52707144 non coding transcript exon variant G/A;C snv 2