Source: GWASCAT ×
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
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 7
rs16991615
MCM8
0.925 0.080 20 5967581 missense variant G/A snv 4.5E-02 4.2E-02 6
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs12294104
LOC102723403
11 30361352 intergenic variant C/T snv 0.14 4
rs16917237
BDNF ; BDNF-AS
11 27680836 intron variant G/T snv 0.16 3
rs707938
MSH5-SAPCD1 ; MSH5 ; SAPCD1
6 31761582 synonymous variant A/G snv 0.38 0.44 3
rs9635759 17 51536424 regulatory region variant G/A snv 0.25 2
rs1799949
BRCA1
17 43093449 synonymous variant G/A snv 0.35 0.31 2
rs4693089
HELQ
4 83452469 intron variant A/G snv 0.60 2
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 2
rs12461110
NLRP11
19 55809297 missense variant G/A snv 0.32 0.26 2
rs7852169
PTGR1 ; ZNF483
9 111556114 intron variant C/G snv 0.15 2
rs1411478
STX6
0.925 0.120 1 180993146 intron variant A/G snv 0.56 2
rs6899676
SYCP2L
6 10895027 intron variant A/G snv 0.21 2
rs9393800
SYCP2L ; LOC101928191
6 10951504 intron variant A/G snv 0.20 2
rs2679894
TGFBRAP1
2 105254322 upstream gene variant A/G snv 0.43 2
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 2
rs365132
UIMC1
5 176951573 synonymous variant G/T snv 0.51 0.58 2
rs11245450
ZRANB1
10 124969506 intron variant G/A snv 0.35 2
rs10145469 14 97303497 intergenic variant C/A snv 5.7E-02 1
rs10496265 2 81441684 intergenic variant T/C snv 0.12 1
rs10734411 11 32520238 intergenic variant G/A snv 0.56 1
rs10852344 16 11923062 upstream gene variant C/T snv 0.43 1