Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6026748
ZNF831
20 59170760 intron variant G/A snv 0.14 3
rs66658258
COL9A3
20 62831150 non coding transcript exon variant G/C;T snv 0.14 3
rs115893283 20 56829109 intergenic variant C/T snv 4.8E-02 2
rs4260308 20 10981537 intron variant G/A snv 0.41 2
rs459588
ZNF831
20 59139712 intron variant A/C snv 0.21 2
rs6129880 20 41623190 upstream gene variant T/C;G snv 2
rs73306888
ZNF831
20 59173534 intron variant G/A snv 0.14 2
rs80346118
PREX1
20 48794612 intron variant G/A snv 0.13 2
rs1040922 20 10787163 intron variant G/T snv 0.27 1
rs1232482
BTBD3
20 11905995 intron variant C/T snv 0.34 1
rs13040824 20 2245223 intron variant G/A snv 0.22 1
rs13042148
PXMP4
20 33710480 intron variant C/T snv 9.6E-02 1
rs237485
KCNB1 ; LOC105372649
20 49387701 intron variant A/G snv 0.34 1
rs2618647 20 17901808 upstream gene variant A/G snv 0.56 1
rs3063286
SLX4IP
20 10507905 intron variant TA/-;TATA;TATATA;TATATATA;TATATATATA delins 1
rs369386096
CST13P
20 23521492 intron variant C/G snv 1.1E-04 1
rs3790228
SLC24A3
20 19488506 intron variant T/G snv 0.25 1
rs6019378
PREX1
20 48693178 intron variant C/T snv 0.48 1
rs6060114 20 31581870 downstream gene variant T/C snv 0.31 1
rs6062621
TCEA2
20 64051912 intron variant G/C;T snv 1
rs6095241
PREX1
20 48692260 intron variant G/A snv 0.49 1
rs6108168
PLCB1 ; LOC105372521
20 8645624 intron variant C/A snv 0.35 1
rs80139154
LINC01752
20 10746012 intron variant T/C snv 4.8E-02 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25