Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143020224
SMARCA4
19 11076648 intron variant C/G;T snv 2
rs112374545
SMARCA4
19 11078223 intron variant C/T snv 0.11 2
rs73015011
SMARCA4
19 11079088 missense variant T/C snv 0.13 2
rs113190300 19 11080015 downstream gene variant C/A;G;T snv 2
rs114846969 19 11080521 downstream gene variant G/A snv 0.12 1
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 2
rs114197570 19 11085594 upstream gene variant C/T snv 3.3E-03 2
rs12151108 19 11086585 upstream gene variant G/A snv 0.12 1
rs17249141
LDLR
19 11089332 upstream gene variant C/T snv 3.3E-03 3
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 2
rs72658860
LDLR
1.000 0.080 19 11110681 missense variant G/A snv 8.8E-04 3.9E-03 1
rs11669576
LDLR ; MIR6886
0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 1
rs5930
MIR6886 ; LDLR
0.827 0.200 19 11113589 synonymous variant A/G snv 0.63 0.66 1
rs2738446
LDLR
19 11116650 intron variant C/A;G snv 0.34 1
rs688
LDLR
0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 2
rs2738452
LDLR
19 11118542 intron variant A/G snv 0.34 1
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs2738464
SPC24 ; LDLR
1.000 0.120 19 11131631 3 prime UTR variant G/C snv 0.82 0.80 2
rs7258950
SPC24
19 11139463 intron variant A/G;T snv 2
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs34774090
SPC24
19 11143211 intron variant A/- delins 0.77 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10