Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9281492
HCP5
6 31473191 intron variant -/T delins 0.33 1
rs5839768
BOK
2 241561143 intron variant -/T;TGCT ins 0.53 1
rs111470917
ADAMTSL3
15 83916786 intron variant -/TAAA delins 1
rs34322845
CRADD
12 93790493 intron variant -/TAAC ins 1
rs35208145 6 80750319 intergenic variant -/TAAC delins 0.11 1
rs11270967 8 56292882 regulatory region variant -/TGTATTATCTTTTGTTTAAACCTTAGCCTT delins 1
rs11323064 11 69465339 upstream gene variant A/- del 0.21 1
rs138647241
VTA1
6 142194305 intron variant A/- del 0.20 1
rs34001204
LOC105373880 ; PNKD ; LOC105373881
2 218314933 intron variant A/- del 0.44 1
rs113168705
ZNF346
5 177081190 downstream gene variant A/-;AA;AAA delins 1
rs11463901 5 171753429 intergenic variant A/-;AA;AAA delins 1
rs397954080
PTPN14
1 214436403 intron variant A/-;AA;AAA delins 1
rs398121251
KIZ
20 21243309 intron variant A/-;AA;AAA delins 1
rs201794926
PPP1R16A
8 144485527 intron variant A/-;AA;AAA;AAAA delins 2
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 7
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 5
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 4
rs10974438
GLIS3
0.925 0.120 9 4291928 intron variant A/C snv 0.29 3
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 3
rs1818782
DAB2 ; C9
5 39424526 intron variant A/C snv 0.56 3
rs2131371
LOC100288798
1.000 12 46402739 intron variant A/C snv 0.77 3
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 3
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 3
rs10152591
DRAIC ; LOC107984788
15 69755818 intron variant A/C snv 9.8E-02 2