Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3130253
MOG
0.925 0.120 6 29666235 missense variant A/G;T snv 0.95; 4.1E-06 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs3134943
AGPAT1 ; MIR6833 ; RNF5
0.882 0.240 6 32179984 intron variant T/A;C snv 0.89 3
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 3
rs3094609
HCG27
0.925 0.080 6 31197789 non coding transcript exon variant T/C snv 0.86 0.89 5
rs760293
BAG6
1.000 0.080 6 31644000 intron variant T/C snv 0.84 0.81 1
rs3129941
TSBP1 ; TSBP1-AS1
0.882 0.240 6 32369909 missense variant A/G;T snv 0.81 3
rs1728785
ZFP90
0.925 0.120 16 68557327 intron variant A/C;T snv 0.77; 7.8E-06 2
rs630379
NELFE ; CYP21A2
0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs535586
EHMT2 ; CYP21A2
0.882 0.160 6 31892560 splice region variant T/A;C snv 0.77 3
rs486416
CYP21A2 ; EHMT2
0.925 0.160 6 31888293 intron variant G/A snv 0.77 0.76 2
rs659445
EHMT2 ; CYP21A2 ; C2
0.882 0.160 6 31896527 intron variant G/A;C snv 0.77 0.76 3
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs3130981
CDSN ; PSORS1C1
0.925 0.080 6 31116036 missense variant T/C;G snv 0.76 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs6795970
SCN10A
0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 2
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 3
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs9268832
HLA-DRB9
0.882 0.160 6 32460012 non coding transcript exon variant T/C snv 0.61 0.59 4
rs660550
SLC44A4 ; CYP21A2
0.882 0.160 6 31869500 intron variant C/A;G snv 0.60 3
rs2242665
CYP21A2 ; SLC44A4
0.882 0.160 6 31871532 missense variant C/T snv 0.60 0.60 3
rs644827
SLC44A4 ; CYP21A2
0.882 0.160 6 31870664 missense variant T/C snv 0.60 0.60 3
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 1