Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2287921
RASIP1
1.000 0.040 19 48725015 non coding transcript exon variant T/C snv 0.37 4
rs10858583
LOC107984478
1.000 0.040 12 87334666 intergenic variant C/T snv 0.79 3
rs12149074
LOC105371357
1.000 0.040 16 80071969 intron variant C/A;G snv 3
rs13086738
SOX2-OT
1.000 0.040 3 181080939 intron variant A/G snv 0.21 3
rs1805576
FXR1
1.000 0.040 3 180949777 intron variant C/G;T snv 0.24 3
rs3818253
TRPC4AP
1.000 0.040 20 35009073 intron variant G/A snv 0.19 3
rs4148087
ABCG1
1.000 0.040 21 42202157 intron variant G/A;T snv 3
rs4854912
SOX2-OT
1.000 0.040 3 181063312 intron variant C/T snv 0.15 3
rs10457441 1.000 0.040 6 98124244 intron variant T/A;C snv 2
rs10875914
KMT2D
1.000 0.040 12 49028311 intron variant A/G snv 0.44 2
rs10994443
ANK3
1.000 0.040 10 60635760 intron variant G/A snv 0.11 2
rs116951791 1.000 0.040 8 92207493 intergenic variant A/G snv 1.0E-02 2
rs12206087 1.000 0.040 6 98135024 intron variant G/A snv 0.39 2
rs12300899
LOC105370052
1.000 0.040 12 125062029 upstream gene variant C/T snv 0.14 2
rs12772424
TCF7L2
1.000 0.040 10 113120792 intron variant A/T snv 0.57 2
rs147721431 1.000 0.040 5 93007488 intergenic variant C/T snv 1.0E-02 2
rs150404479
CFAP57 ; EBNA1BP2 ; LOC105378685
1.000 0.040 1 43222879 missense variant T/C snv 9.1E-03 9.8E-03 2
rs17018311
INTS7
1.000 0.040 1 211981666 intron variant T/C snv 2.7E-02 2
rs17541406
LOC105370982
1.000 0.040 15 93346230 intron variant C/A;G;T snv 2
rs17826816
ADCY2
1.000 0.040 5 7519185 intron variant A/G snv 0.17 2
rs1985671
FBLN1
1.000 0.040 22 45566024 intron variant G/T snv 0.65 2
rs2273684
GSS
1.000 0.040 20 34941963 intron variant T/G snv 0.52 2
rs290475
TCF7L2
1.000 0.040 10 113114260 intron variant C/A;T snv 2
rs416350
LINC02384
1.000 0.040 12 68385633 intron variant G/A;T snv 2
rs58630086
ALOX12-AS1 ; ALOX12P2
1.000 0.040 17 6878094 intron variant G/A;C snv 2