Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 1
rs9387478
DCBLD1
0.851 0.080 6 117465017 intron variant C/A;T snv 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 1
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 4
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 4
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47 1
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs9480192
LOC105378054
1.000 0.040 6 150305155 intergenic variant C/A;G;T snv 1
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs12503223
LDB2
1.000 0.040 4 16841093 intron variant G/A snv 0.18 1
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 1
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 1
rs13314271
TP63
0.925 0.080 3 189639813 intron variant T/C snv 0.45 1
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 1
rs2151280
CDKN2B-AS1
0.701 0.360 9 22034720 non coding transcript exon variant G/A snv 0.46 3
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 1
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 5
rs3129791
HCG15
0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 4
rs3130893 0.882 0.160 6 29012930 intergenic variant A/G snv 5.3E-02 3