Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs10138752
RAD51B
14 68713254 intron variant C/T snv 8.8E-02 5
rs10171849
IL1RN
2 113108257 intron variant A/C snv 0.35 1
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs10206089 2 61476184 intron variant G/A snv 4
rs1025687
MAPK4
18 50621423 intron variant T/C snv 0.61 3
rs1025688
MAPK4
18 50621506 intron variant G/A snv 0.35 3
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs10995477
JMJD1C
10 63250912 intron variant T/C snv 0.43 4
rs11104881 12 88449697 intergenic variant T/A;C snv 1
rs11137087 8 7048518 intergenic variant A/G snv 0.60 2
rs111930700
ACVR1B
12 51967869 intron variant C/G snv 8.4E-02 4
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs11361923
NOXRED1
14 77396337 intron variant C/- delins 0.54 4
rs113977268
CASC15 ; LOC105374971
6 22359286 intron variant G/A snv 5.7E-02 2
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs11405616
NDFIP1
5 142130697 intron variant A/-;AA;AAA;AAAA delins 4
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs115681968
HLA-B ; LOC112267902
6 31304776 intron variant G/A snv 1
rs11625487
ISM2
14 77495266 intron variant G/A;C snv 0.70 2
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5