Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1261070
TCF4
1.000 0.040 18 55235854 intron variant A/G snv 0.94 2
rs12967855
CELF4
1.000 0.040 18 37558282 intron variant A/G snv 0.52 2
rs1560312
MAPT
1.000 0.040 17 45901622 intron variant A/G snv 0.29 2
rs1724422
LINC02210-CRHR1
1.000 0.040 17 45699947 intron variant A/G snv 0.47 2
rs17570807 1.000 0.040 18 37662673 intron variant A/G snv 3.1E-02 2
rs17711053
VWC2L
1.000 0.040 2 214574984 intron variant A/G snv 0.11 2
rs2298489
TTC12
1.000 0.040 11 113364697 splice region variant A/G snv 0.61 2
rs2396133 1.000 0.040 7 109557010 intron variant A/G snv 0.47 2
rs28893517
GABBR1
1.000 0.040 6 29597596 intron variant A/G snv 6.6E-02 2
rs3758667
DDB2
1.000 0.040 11 47214747 intron variant A/G snv 0.69 2
rs3936093
LINGO1
1.000 0.040 15 77809567 intron variant A/G snv 0.47 2
rs57043326
C6orf99
1.000 0.040 6 158893901 intron variant A/G snv 5.2E-02 2
rs59382200
LOC105374054
1.000 0.040 3 117240427 intergenic variant A/G snv 0.29 2
rs62199592 2 183858773 intergenic variant A/G snv 2.1E-02 2
rs7502590
BAIAP2
1.000 0.040 17 81108281 non coding transcript exon variant A/G snv 0.14 2
rs75507262
LINC02815
1.000 0.040 1 229213737 intergenic variant A/G snv 8.0E-03 2
rs77087420
KIAA1109
1.000 0.040 4 122201701 intron variant A/G snv 3.4E-02 2
rs913687
RABGAP1L
1.000 0.040 1 174805993 intron variant A/G snv 0.60 2
rs9904290
LOC105371800 ; MAPT
1.000 0.040 17 45924905 intron variant A/G snv 0.53 2
rs11123857
NPAS2
2 100987350 non coding transcript exon variant A/G snv 0.29 1
rs7713917 0.925 0.040 5 79533426 upstream gene variant A/G snv 0.54 1
rs11693031
ERBB4
1.000 0.040 2 211813206 intron variant A/G;T snv 2
rs297346
SOX6
1.000 0.040 11 16334225 intron variant A/G;T snv 2
rs60393230
LOC107987122
1.000 0.040 9 119893005 intergenic variant A/G;T snv 2
rs62183032
ERBB4
1.000 0.040 2 211774137 intron variant A/G;T snv 2