Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149310
ABCA1
9 104826853 intron variant A/T snv 0.34 3
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs944801
CDKN2B-AS1
0.882 0.120 9 22051671 intron variant G/A;C snv 3
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 2
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs113533135
LRP1B
1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs113805659
MAGI2
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs12040333
ST3GAL3
1.000 0.080 1 43848369 intron variant G/A;C snv 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs1333037
CDKN2B-AS1
0.925 0.040 9 22040766 intron variant C/T snv 0.71 2
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 2
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 2
rs1440581
PPM1K-DT
1.000 0.080 4 88305270 intron variant T/A;C snv 2
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs1532002
LRP1B
1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs17214144
OSBPL3
1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs1912826
KLKB1
4 186228386 intron variant G/A;C snv 2
rs2657880
SPRYD4
12 56469986 3 prime UTR variant G/C snv 0.15 2