Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs12374521
LOC107986462 ; HTR4
5 148457317 intron variant C/T snv 0.45 4
rs1490384 6 126530014 intron variant C/G;T snv 4
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 4
rs900145 11 13272358 upstream gene variant C/T snv 0.62 4
rs13322435 3 157077679 upstream gene variant A/G snv 0.46 3
rs1659127 16 14294448 intergenic variant G/A;C;T snv 3
rs16917237
BDNF ; BDNF-AS
11 27680836 intron variant G/T snv 0.16 3
rs2206271
TFAP2B
6 50818295 upstream gene variant T/A snv 0.32 3
rs246185
MIR193BHG
16 14301575 intron variant T/C snv 0.34 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs314268
LIN28B
6 104970103 intron variant G/A snv 0.64 3
rs4549631 6 126645162 intron variant T/C;G snv 3
rs4929923
TRIM66
11 8617653 3 prime UTR variant T/C snv 0.59 3
rs707938
MSH5-SAPCD1 ; MSH5 ; SAPCD1
6 31761582 synonymous variant A/G snv 0.38 0.44 3
rs7846385 8 77247943 intergenic variant T/C snv 0.23 3
rs9391253
LIN28B-AS1
6 104919741 intron variant A/T snv 0.29 3
rs9393800
SYCP2L ; LOC101928191
6 10951504 intron variant A/G snv 0.20 3
rs10156597
LINC01505
9 106179228 intron variant A/T snv 0.36 2
rs10780649
LOC101927575
9 84088646 intron variant T/G snv 0.64 2
rs10980926
ZNF483
9 111531354 intron variant A/G snv 0.56 2
rs11209943
LOC105378797
1 72284817 intron variant A/G snv 0.53 2
rs1172955 10 96117563 downstream gene variant T/A snv 0.60 2