Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8041357
ARID3B
0.882 0.120 15 74577097 intron variant T/C snv 6.6E-02 3
rs8102137 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 3
rs8444
CERS2
0.882 0.120 1 150966095 3 prime UTR variant G/A snv 0.35 3
rs861531
XRCC3 ; LOC112268131 ; KLC1
0.882 0.120 14 103706470 3 prime UTR variant C/A snv 0.32 3
rs921142 0.882 0.120 8 41311757 upstream gene variant T/C snv 0.31 3
rs9624880
GRK3
0.882 0.120 22 25588025 intron variant C/T snv 3
rs9913017
SLC39A11
0.882 0.120 17 73014881 intron variant A/C;T snv 3
rs150799650
CYP1B1 ; CYP1B1-AS1
0.925 0.120 2 38073618 non coding transcript exon variant G/T snv 7.0E-05 2
rs1937920 0.925 0.120 10 5119763 downstream gene variant A/G snv 0.28 2
rs2836007
KCNJ6
0.925 0.120 21 37834589 intron variant C/T snv 0.21 2
rs4510656
CDKAL1
0.925 0.120 6 20766466 intron variant C/A snv 0.39 2
rs5003154
PAG1
0.925 0.120 8 81074718 intron variant T/C;G snv 2
rs6104690
LINC02871
0.925 0.120 20 11007451 intron variant G/A;T snv 2
rs7238033
SLC14A1 ; LOC105372093
0.925 0.120 18 45737001 intron variant T/C snv 0.61 2
rs7747724
CDKAL1
0.925 0.120 6 20751084 intron variant T/C snv 0.41 2
rs2204008 1.000 0.120 12 38045401 intergenic variant C/A;T snv 1
rs28897728
BRCA2
1.000 0.120 13 32338940 missense variant G/A snv 3.9E-04 4.3E-04 1
rs4813953
LINC02871
1.000 0.120 20 11010490 intron variant T/C snv 0.63 1
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs12628
LRRC56 ; HRAS
0.776 0.160 11 534242 synonymous variant A/G snv 0.32 0.34 10
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs710886
LOC105375751 ; PCAT1
0.763 0.160 8 127014615 intron variant C/T snv 0.37 9
rs1883965
MTOR
0.807 0.160 1 11262099 intron variant A/G snv 0.63 8
rs125701
OGG1
0.790 0.160 3 9748794 upstream gene variant G/A snv 0.13 7
rs16901904
PCAT1 ; LOC105375751
0.790 0.160 8 127015257 intron variant T/C snv 0.27 7