Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50 13
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs4360494
SF3A3
0.776 0.080 1 37990219 upstream gene variant G/C snv 0.45 12
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs6584283
LINC01475
0.776 0.080 10 99530544 intron variant T/C snv 0.56 12
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs1412834
CDKN2B-AS1
0.790 0.080 9 22110132 intron variant T/C snv 0.64 11
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs35446936
ACTRT3
0.776 0.080 3 169768720 intron variant G/A snv 0.21 11
rs6063514 0.776 0.080 20 50438781 intergenic variant C/T snv 0.42 11
rs10049390
SLCO2A1
0.776 0.080 3 133982275 intron variant G/A snv 0.67 10
rs10457678
ECT2L
0.790 0.080 6 138801103 intron variant A/G snv 0.19 10
rs10511330
ZBTB20
0.776 0.080 3 114402172 intron variant T/C snv 0.22 10
rs1078643
TMEM220-AS1 ; TMEM238L
0.776 0.080 17 10803924 missense variant G/A;C snv 10
rs10849433
LOC105369624
0.776 0.080 12 6297738 regulatory region variant T/C snv 0.38 10
rs10980628
LPAR1
0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs11085466
LOC101929007
0.790 0.080 19 21569009 intron variant G/C snv 0.23 10
rs11087784 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 10
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs11196170
TCF7L2
0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 10