Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5860563
ADH4 ; LOC100507053
1.000 0.080 4 99126006 intron variant -/A delins 3
rs58598658
KLF12
0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs143894582
PTPN11
1.000 0.080 12 112469070 intron variant A/-;AA delins 1
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs1709819
KCNJ6
1.000 0.080 21 37663813 intron variant A/C snv 0.59 3
rs1709820
KCNJ6
1.000 0.080 21 37663669 intron variant A/C snv 0.57 3
rs1787396
KCNJ6
1.000 0.080 21 37664185 intron variant A/C snv 0.57 3
rs1787398
KCNJ6
1.000 0.080 21 37665202 intron variant A/C snv 0.57 3
rs2835836
KCNJ6
1.000 0.080 21 37616885 3 prime UTR variant A/C snv 0.26 3
rs4384980 1.000 0.080 3 182741281 upstream gene variant A/C snv 0.48 1
rs7183893
LINC02694
1.000 0.080 15 38704780 intron variant A/C snv 0.23 1
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 4
rs1709835
KCNJ6
1.000 0.080 21 37665334 intron variant A/C;G snv 0.57 3
rs1787404
KCNJ6
1.000 0.080 21 37677060 intron variant A/C;G snv 3
rs9378160
MICB
1.000 0.080 6 31500215 intron variant A/C;G snv 3
rs29230
GABBR1
0.807 0.440 6 29608616 missense variant A/C;G snv 4.1E-06; 0.18 1
rs12898370
HMG20A
1.000 0.080 15 77516256 intergenic variant A/C;T snv 3
rs1787395
KCNJ6
1.000 0.080 21 37664176 intron variant A/C;T snv 3
rs6701037 1.000 0.080 1 175150943 downstream gene variant A/C;T snv 3
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs11825659
IGSF9B
0.925 0.080 11 133925624 intron variant A/G snv 0.12 4
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
rs10211296
CSRNP3
1.000 0.080 2 165633833 intron variant A/G snv 0.34 3