Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28549760
BTC
1.000 0.080 4 74794307 missense variant A/C snv 0.19 0.25 1
rs28869187
NFYA ; OARD1
1.000 0.080 6 41088766 intron variant A/C snv 2.9E-02 1
rs2943640 1.000 0.080 2 226228869 intergenic variant A/C snv 0.75 1
rs4567661
RASGRP1
1.000 0.080 15 38493913 non coding transcript exon variant A/C snv 0.33 1
rs4710940
CDKAL1
1.000 0.080 6 20657781 intron variant A/C snv 0.46 1
rs527320094
LOC105378797
1.000 0.080 1 72387303 intron variant A/C snv 4.1E-04 1
rs5929706 1.000 0.080 X 135935372 intergenic variant A/C snv 1
rs6103716
HNF4A
1.000 0.080 20 44370990 intron variant A/C snv 0.37 1
rs6515236
LOC105372562
1.000 0.080 20 22455111 intron variant A/C snv 0.37 1
rs6593976
SLC26A9-AS1 ; SLC26A9
1.000 0.080 1 205940157 intron variant A/C snv 0.56 1
rs77464186
ARAP1
1.000 0.080 11 72749353 intron variant A/C snv 0.12 1
rs7754586
ENPP1
1.000 0.080 6 131891602 3 prime UTR variant A/C snv 0.30 1
rs77820034 1.000 0.080 15 62094596 regulatory region variant A/C snv 6.1E-03 1
rs78627331
EXOC6
1.000 0.080 10 93052497 intron variant A/C snv 4.5E-04 1
rs7988007 1.000 0.080 13 58414137 intergenic variant A/C snv 0.14 1
rs9271774 1.000 0.080 6 32626532 upstream gene variant A/C snv 0.76 1
rs9358358
CDKAL1
1.000 0.080 6 20719162 intron variant A/C snv 0.19 1
rs14259
PSMD9
0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs1057910
CYP2C9
0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs4923461
BDNF-AS ; LINC00678
0.925 0.120 11 27635363 intron variant A/C;G snv 5
rs7107217 0.882 0.160 11 129603795 intron variant A/C;G snv 3
rs352165
ALAS1
0.925 0.120 3 52208886 intron variant A/C;G snv 0.47 2