Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 3
rs6759892
UGT1A6 ; UGT1A9 ; UGT1A7 ; UGT1A8 ; UGT1A10
0.851 0.160 2 233693023 missense variant T/G snv 0.39 0.39 3
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 2
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1
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
rs13314271
TP63
0.925 0.080 3 189639813 intron variant T/C snv 0.45 1
rs1846594 0.925 0.120 3 113197356 intergenic variant G/A;T snv 1
rs1899951
PPARG
0.851 0.160 3 12353341 intron variant C/T snv 0.26 1
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 1
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 1
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs1489759
LOC105377462
0.882 0.080 4 144553321 intron variant A/G snv 0.43 2
rs17021918
PDLIM5
0.776 0.240 4 94641726 intron variant C/T snv 0.30 2
rs7689420
HHIP-AS1 ; HHIP
0.851 0.080 4 144647200 non coding transcript exon variant T/C snv 0.79 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9