Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201205097 2 613044 intergenic variant -/AC delins 1
rs35212912
DLGAP1
18 3816054 intron variant -/C ins 1
rs11349289
ATRNL1
10 115724059 intron variant A/- delins 0.36 1
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs241036
LINC02210 ; LINC02210-CRHR1
17 45654353 non coding transcript exon variant A/C snv 0.14 2
rs10150590 14 40456677 intergenic variant A/C snv 0.63 1
rs11022756
ARNTL
11 13293892 intron variant A/C snv 0.65 1
rs11215400
CADM1
11 115181915 intron variant A/C snv 0.21 1
rs11792861
MIR32 ; TMEM245
9 109047015 intron variant A/C snv 0.22 1
rs12167144
EIF4HP2 ; OSBP2 ; LOC107985544
22 30902221 non coding transcript exon variant A/C snv 0.36 1
rs12193842
SNAP91
6 83612439 intron variant A/C snv 0.31 1
rs12656569 5 169311587 intergenic variant A/C snv 0.79 1
rs1461503 11 122974367 downstream gene variant A/C snv 0.51 1
rs1482582 4 103730396 intergenic variant A/C snv 0.34 1
rs28672845 3 88221477 regulatory region variant A/C snv 0.69 1
rs6010651
ZBTB46
20 63786890 intron variant A/C snv 0.43 1
rs6136033
PCSK2 ; LOC105372546
20 17227859 intron variant A/C snv 0.56 1
rs62415601 6 75722400 downstream gene variant A/C snv 0.27 1
rs6589964 11 122999975 intergenic variant A/C snv 0.54 1
rs7113019
JHY
11 122948411 intron variant A/C snv 0.55 1
rs72992070 11 115153970 intergenic variant A/C snv 0.19 1
rs7617480
KLHDC8B
3 49173299 intron variant A/C snv 0.76 1
rs9295482
CDKAL1
6 20761003 intron variant A/C snv 0.29 1
rs929843
PDXDC2P ; PDXDC2P-NPIPB14P
16 70011845 non coding transcript exon variant A/C snv 0.84 1