Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs72959041
RSPO3
6 127133748 intron variant G/A snv 3.2E-02 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10842707 12 26318431 intron variant C/G;T snv 4