Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs10956838 1.000 0.040 8 92392214 intergenic variant A/C snv 0.28 2
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs7164335
ITGA11
1.000 0.040 15 68422693 intron variant A/C;G snv 1
rs4916723
LINC00461
0.925 0.040 5 88558577 intron variant A/C;G;T snv 2
rs12042052 1.000 0.040 1 232799973 upstream gene variant A/C;G;T snv 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 5
rs11162556 0.925 0.040 1 78795698 intergenic variant A/G snv 0.32 2
rs145108385
LOC648987
0.925 0.040 5 43054645 intron variant A/G snv 2
rs2782639
PTPRF
0.925 0.040 1 43540668 intron variant A/G snv 0.26 2
rs325485
LOC105379109
0.925 0.120 5 104659667 intron variant A/G snv 0.65 2
rs74760947 0.925 0.040 8 34495092 intergenic variant A/G snv 3.1E-02 2
rs797267 0.925 0.040 12 89373460 intron variant A/G snv 0.28 2
rs11243897
AK8
1.000 0.040 9 132742896 intron variant A/G snv 0.33 1
rs1278352
ADAM12
1.000 0.040 10 126084807 intron variant A/G snv 0.61 1
rs142295881
MLIP
1.000 0.040 6 54034290 intron variant A/G snv 1.1E-02 1
rs1427829 1.000 0.040 12 89366967 intron variant A/G snv 0.46 1
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 1