Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16841143
PTH2R
2 208384849 intron variant G/A snv 0.13 2
rs182087934 2 183742707 intergenic variant G/A snv 2
rs384005
MEF2C-AS2
5 88709286 intron variant T/C snv 0.70 2
rs4554696
PDE4B
1 65942328 intron variant C/T snv 0.33 2
rs62199592 2 183858773 intergenic variant A/G snv 2.1E-02 2
rs6475417
SLC24A2
9 20212043 intergenic variant A/G;T snv 2
rs6661750
PDE4B
1 66081201 intron variant A/G;T snv 2
rs11123857
NPAS2
2 100987350 non coding transcript exon variant A/G snv 0.29 1
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs7107356 1.000 0.040 11 47654618 downstream gene variant A/G snv 0.45 4
rs754593
MAPT
1.000 0.040 17 45977330 non coding transcript exon variant G/A snv 0.52 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs10965780 1.000 0.040 9 23341717 intron variant C/G;T snv 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs113378111 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 3
rs114465512
IGLV10-54
1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 3
rs117198528
LOC105372112
1.000 0.040 18 49694188 intergenic variant T/G snv 1.0E-02 3
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs12963463
TCF4
1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs138472420
BICRA
1.000 0.040 19 47657765 intron variant G/A snv 3.3E-03 3
rs141746753 1.000 0.040 8 56934154 intergenic variant C/T snv 3.1E-03 3
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3