Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1056198
RNF114
0.925 0.040 20 49939692 intron variant C/T snv 0.34 2
rs12445568
STX1B
0.925 0.040 16 30993491 splice region variant T/C snv 0.39 0.38 2
rs12884468 0.925 0.040 14 35383280 downstream gene variant T/C snv 0.47 2
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 2
rs2066819
STAT2
0.925 0.040 12 56356420 intron variant C/T snv 4.9E-02 4.5E-02 2
rs2233278
TNIP1
0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 2
rs2675662
CAMK2G
0.925 0.040 10 73839369 intron variant A/G snv 0.55 2
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 2
rs3802826
ETS1
0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv 2
rs4406273
LOC112267902 ; HLA-B ; LINC02571
0.925 0.040 6 31298313 intron variant G/A snv 8.6E-02 2
rs4685408
PLCL2
0.925 0.040 3 16954543 intron variant G/A snv 0.56 2
rs62149416
LINC01185
0.925 0.040 2 60856371 intron variant T/C snv 0.26 2
rs7536201
RUNX3
0.925 0.040 1 24966593 upstream gene variant T/C;G snv 2
rs7637230
LINC02085
0.925 0.040 3 101944711 intron variant A/G;T snv 2
rs7709212
LOC285626
0.925 0.040 5 159337169 intron variant T/C snv 0.34 2
rs892085
QTRT1
0.925 0.040 19 10707416 intron variant G/A snv 0.57 0.59 2
rs11652075
CARD14 ; SGSH
0.882 0.040 17 80205094 missense variant C/T snv 0.41 0.40 1
rs12489120
BHLHE40 ; BHLHE40-AS1
1.000 0.040 3 4978778 intron variant C/A;G;T snv 1
rs2675669 1.000 0.040 10 73894114 intergenic variant C/T snv 0.55 1
rs4712528
CDKAL1
1.000 0.040 6 20678199 intron variant G/C;T snv 1
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs9394026
MUC22
1.000 0.040 6 31014767 intron variant G/A snv 0.24 1
rs1250544
ZMIZ1
0.882 0.080 10 79273128 intron variant G/A snv 0.32 3
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 3
rs181359
UBE2L3
0.882 0.080 22 21574352 intron variant G/A snv 0.21 2