Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs10519198
IREB2
0.925 0.080 15 78450412 intron variant C/A;G snv 2
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 1
rs1052486
BAG6
0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 1
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 4
rs10849605
RAD52
0.882 0.080 12 955272 intron variant T/C snv 0.49 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 2
rs11072768
CHRNB4
0.882 0.080 15 78637136 intron variant T/C;G snv 1
rs11072793
CHRNB4 ; LOC105370913 ; LOC112268142
1.000 0.080 15 78714100 intron variant G/A snv 0.58 2
rs11090598
HORMAD2
1.000 0.080 22 30125781 intron variant A/G snv 0.21 1
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 1
rs1150735
RNF39
0.925 0.200 6 30077422 upstream gene variant G/A snv 0.30 2
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 2
rs11637630
CHRNA3
0.882 0.080 15 78607377 intron variant G/A snv 0.71 1
rs11638372
LOC112268142 ; CHRNB4
0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 3
rs11658063
HNF1B
0.851 0.120 17 37743881 intron variant G/C;T snv 1
rs1169300
HNF1A
0.882 0.080 12 120993422 intron variant G/A snv 0.27 1