Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1912826
KLKB1
4 186228386 intron variant G/A;C snv 2
rs1998013 1 55492357 intron variant C/T snv 4.4E-03 1
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 3
rs2168889 4 74357994 intergenic variant A/G snv 4.7E-02 1
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 4
rs2306786
MYO1E
15 59195731 intron variant C/G snv 8.0E-02 1
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 1
rs2390582
LOC105378851
1 90478350 intergenic variant A/G snv 0.15 1
rs2657880
SPRYD4
12 56469986 3 prime UTR variant G/C snv 0.15 2
rs2680830
VSNL1
1.000 0.080 2 17596817 intron variant A/G;T snv 0.94 2
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 4
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 2
rs3798722
ELOVL2
6 11040190 intron variant A/G snv 0.39 1
rs3809346
COL4A1 ; COL4A2
1.000 0.080 13 110308596 intron variant G/A;C snv 1
rs4149310
ABCA1
9 104826853 intron variant A/T snv 0.34 3
rs4272321
PTPRN2
1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 5
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 2
rs4788815
LOC105371334
16 71600908 intergenic variant A/T snv 0.69 2
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 3
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs4977575
CDKN2B-AS1
1.000 0.040 9 22124745 intron variant C/G;T snv 1
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 1