Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 17
rs10429489 0.925 0.080 9 21787522 intergenic variant G/A snv 0.26 2
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs1056562
MPZL2
1.000 0.040 11 118254910 3 prime UTR variant T/C snv 0.57 1
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 2
rs10758203 1.000 0.040 9 33421422 intergenic variant G/A;C snv 1
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 17
rs11375254
TP63
0.882 0.080 3 189625454 intergenic variant A/-;AA;AAA;AAAA delins 3
rs114807680
EPHB1
1.000 0.040 3 135085649 intron variant G/A snv 9.8E-03 1
rs114928225 1.000 0.040 2 118692164 intergenic variant T/A snv 1.0E-02 1
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11571818
BRCA2
0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 19
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 1
rs116080888 1.000 0.040 6 32618459 intergenic variant C/A snv 1
rs11610143
ACVR1B
0.925 0.080 12 51955287 intron variant C/G snv 0.18 2
rs11632038
GALK2
1.000 0.040 15 49314101 intron variant A/G snv 0.15 1
rs11638372
LOC112268142 ; CHRNB4
0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 2
rs11639372
CHRNB4 ; LOC112268142
0.925 0.080 15 78674313 intron variant C/T snv 0.30 4
rs116506680 1.000 0.040 6 29813272 upstream gene variant T/A;C;G snv 1