Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 3
rs11781551
LOC105375733
1.000 0.040 8 122395852 intergenic variant G/A snv 0.40 1
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 1
rs17045031
LOC105377142
1.000 0.040 3 66717940 intergenic variant G/A snv 0.10 1
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 1
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 1
rs4888378
CFDP1
0.851 0.040 16 75298143 intron variant A/G snv 0.52 1
rs6601530
PINX1
1.000 0.040 8 10813762 intron variant G/A snv 0.61 1
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 1
rs2229116
RYR3
0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 5
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 5
rs28362286
PCSK9
0.851 0.080 1 55063542 stop gained C/A;T snv 5.6E-04 2
rs67608943
PCSK9
0.851 0.080 1 55046549 stop gained C/G;T snv 1.9E-04 2
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 2
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 1
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 1
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 1
rs4901536
SAMD4A
0.925 0.080 14 54733816 intron variant T/C snv 0.67 1
rs6666258
KCNN3
0.882 0.080 1 154841792 intron variant G/C snv 0.30 1
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 6
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 2
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 2