Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2948097
KAT2B
3 20063934 intron variant A/G snv 0.65 1
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 6
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs8095142
C18orf25
18 46213842 intron variant G/A snv 0.64 2
rs239260
SLC22A20P
11 65216232 intron variant G/A snv 0.64 2
rs8012
SYCE2 ; GCDH
19 12899706 3 prime UTR variant A/G snv 0.61 0.64 2
rs2040494
CDK6
7 92627591 intron variant C/T snv 0.64 2
rs9683085
ATR
3 142529656 intron variant G/A snv 0.64 1
rs131777
SYCE3
22 50552604 intron variant C/T snv 0.63 2
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 6
rs136211
MYH9
22 36362502 intron variant A/G snv 0.62 2
rs9944715
C18orf25
18 46251293 intron variant A/G snv 0.62 3
rs4890633
C18orf25
18 46253312 intron variant G/A snv 0.62 1
rs10766533
CSRP3 ; CSRP3-AS1
11 19203130 intron variant T/A snv 0.62 4
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 5
rs7615316
PLS1 ; LOC105374136
3 142637084 intron variant G/A snv 0.61 2
rs9820353
RPL6P9
3 142581084 intron variant A/G snv 0.61 1
rs7155454
FNTB ; MAX ; CHURC1-FNTB
14 65035521 intron variant G/A snv 0.61 2
rs6147862
LRIG1
3 66402550 intron variant GCATGGTGGGAAGGACCCAAGGT/-;GCATGGTGGGAAGGACCCAAGGTGCATGGTGGGAAGGACCCAAGGT delins 0.60 2
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs1264423
PPP1R10
6 30603694 non coding transcript exon variant T/C snv 0.57 0.60 1
rs4709818
LOC105378102
6 164038343 intergenic variant C/T snv 0.59 3
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs2974760
HBZ
16 152050 intron variant C/A snv 0.58 2