Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12051548
TM4SF5
17 4779740 intron variant G/C snv 7.5E-02 1
rs2306786
MYO1E
15 59195731 intron variant C/G snv 8.0E-02 1
rs59490629
PDSS2
1.000 0.080 6 107256268 intron variant G/A snv 8.5E-02 2
rs8134546
LINC01426
1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 2
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 3
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs9384331
LOC105378054
1.000 0.080 6 150279905 intergenic variant T/C snv 0.12 2
rs12507628 4 72779634 regulatory region variant G/A snv 0.13 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
rs17214144
OSBPL3
1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 4
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs1303
SERPINA1
0.925 0.040 14 94378506 missense variant T/G snv 0.28 0.22 2
rs7804216
ACTR3C
1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs749924
LINC01880
2 242084344 upstream gene variant C/T snv 0.25 1
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 4
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 3
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 2
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 1
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 6
rs4149310
ABCA1
9 104826853 intron variant A/T snv 0.34 3
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 1