Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35295665
CASZ1
1 10737371 intron variant -/C delins 2
rs201445483
SMC6
2 17708820 intron variant -/GT delins 7.3E-05 2
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs11731886
LOC105377506
4 155738667 downstream gene variant A/C snv 0.21 3
rs13405173
PDE1A
2 182449087 intron variant A/C snv 8.8E-03 3
rs12829468
LINC02398
12 20043911 intron variant A/C snv 0.61 2
rs16853958
LOC105371692
1 204559216 downstream gene variant A/C snv 0.59 2
rs259983
ZNF831
20 59160402 5 prime UTR variant A/C snv 0.25 2
rs459588
ZNF831
20 59139712 intron variant A/C snv 0.21 2
rs7302816 12 89556543 upstream gene variant A/C snv 0.27 2
rs9969423
FAM167A-AS1
8 11398066 intron variant A/C snv 0.39 2
rs12292796 11 39404549 intergenic variant A/C snv 0.10 1
rs1525889
TF
3 133771189 intron variant A/C snv 0.29 1
rs17144687 5 118824240 intergenic variant A/C snv 4.5E-02 1
rs4643
PGM1
1 63659768 3 prime UTR variant A/C snv 0.17 1
rs483916 8 9936091 intergenic variant A/C snv 0.51 1
rs4854723 3 133535414 regulatory region variant A/C snv 0.52 1
rs6439431
TF ; INHCAP
3 133729265 intron variant A/C snv 0.38 1
rs8177213
TF ; INHCAP
3 133753383 intron variant A/C snv 0.25 1
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs150844304
TP53BP1
15 43434427 intron variant A/C;G snv 4
rs1111336 2 28435029 regulatory region variant A/C;G snv 2
rs2301054
PGM1
1 63641357 intron variant A/C;G snv 1