Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13211318 0.925 0.040 6 32134903 upstream gene variant A/C snv 0.11 5
rs2524123
HLA-B ; LINC02571 ; LOC112267902
0.925 0.040 6 31297537 intron variant T/C snv 0.34 5
rs3130424 0.925 0.040 6 31250462 intergenic variant A/C;G;T snv 5
rs34214527
TNXB
0.925 0.040 6 32046679 intron variant C/T snv 0.11 5
rs13076312
LPP
1.000 0.040 3 188371466 intron variant C/T snv 0.44 2
rs13091753
LPP
1.000 0.040 3 188396801 intron variant G/C;T snv 2
rs1559810
LPP
1.000 0.040 3 188406566 intron variant C/A snv 0.36 2
rs1635168
HERC2
1.000 0.040 15 28290120 intron variant A/C snv 0.77 2
rs28362683
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32405186 synonymous variant G/A snv 0.12 0.10 2
rs9851967
LPP
1.000 0.040 3 188369840 intron variant C/T snv 0.35 2
rs10768122
SLC1A2
1.000 0.040 11 35259305 3 prime UTR variant A/G snv 0.33 1
rs1079541 1.000 0.040 6 30438979 intergenic variant C/A snv 0.17 1
rs11021232 1.000 0.040 11 95587644 intron variant T/C snv 0.14 1
rs11079035
RAB5C
1.000 0.040 17 42136994 intron variant G/A snv 0.29 1
rs11593576
ZMIZ1
0.925 0.040 10 79256139 intron variant C/T snv 0.29 1
rs11964542
TRIM31 ; TRIM31-AS1
1.000 0.040 6 30103983 non coding transcript exon variant T/C snv 7.2E-02 1
rs11966200
SLC44A4 ; CYP21A2
0.851 0.040 6 31869289 intron variant C/T snv 2.9E-02 4.5E-02 1
rs11966619
LOC105375012
1.000 0.040 6 30461256 intergenic variant T/G snv 0.17 1
rs11967808
TRIM26
1.000 0.040 6 30211411 intron variant G/C snv 3.2E-02 1
rs12201301 1.000 0.040 6 31039780 downstream gene variant G/A snv 2.7E-02 1
rs12206131
LINC01149
1.000 0.040 6 31446233 non coding transcript exon variant A/G snv 1.8E-02 1
rs12206499
HLA-A
1.000 0.040 6 29969350 downstream gene variant A/G snv 0.27 1
rs1264377 1.000 0.040 6 30797130 downstream gene variant G/A snv 0.13 1
rs1265181
PSORS1C3
0.925 0.040 6 31188008 intergenic variant G/C snv 0.15 1
rs13118
NEU1
1.000 0.040 6 31859509 3 prime UTR variant A/G;T snv 1