Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs4889
KISS1
0.882 0.160 1 204190659 missense variant G/A;C snv 5.2E-06; 0.29 5
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv 5
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 5
rs1490384 6 126530014 intron variant C/G;T snv 4
rs900145 11 13272358 upstream gene variant C/T snv 0.62 4
rs4243084
CHRNA3
1.000 0.040 15 78619330 intron variant G/C snv 0.30 4
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 4
rs12374521
LOC107986462 ; HTR4
5 148457317 intron variant C/T snv 0.45 4
rs951366
NUCKS1
0.925 0.240 1 205716224 3 prime UTR variant T/C snv 0.34 4
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 4
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 3
rs13322435 3 157077679 upstream gene variant A/G snv 0.46 3
rs1659127 16 14294448 intergenic variant G/A;C;T snv 3
rs4549631 6 126645162 intron variant T/C;G snv 3
rs7821178 0.925 0.080 8 77181601 intergenic variant C/A;G;T snv 3
rs7846385 8 77247943 intergenic variant T/C snv 0.23 3
rs999885
AP4M1 ; MCM7
0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 3
rs16917237
BDNF ; BDNF-AS
11 27680836 intron variant G/T snv 0.16 3
rs1254337
C14orf39
0.925 0.120 14 60453807 intron variant A/T snv 0.37 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs314268
LIN28B
6 104970103 intron variant G/A snv 0.64 3
rs314280
LIN28B
0.925 0.040 6 104952962 intron variant A/G snv 0.46 3