Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12274302
DISC1FP1
1.000 11 90853732 non coding transcript exon variant C/A;G;T snv 4
rs2071473
HLA-DOB
1.000 6 32814828 intron variant C/G;T snv 4
rs2280801
PRRC2A
1.000 6 31624287 missense variant C/A;T snv 4.0E-06; 6.5E-02 4
rs2507976 1.000 6 31384110 upstream gene variant C/A;T snv 4
rs2518028
HCP5
1.000 6 31468270 non coding transcript exon variant T/A;C snv 4
rs3093553
LTB
1.000 6 31581779 non coding transcript exon variant T/C;G snv 4.1E-06; 6.0E-02 4
rs3094211
PSORS1C1 ; CDSN
1.000 6 31118625 non coding transcript exon variant G/A;C snv 4
rs3095234
MICB-DT ; MICB
1.000 6 31496794 intron variant C/A;T snv 4
rs3095320
CDSN ; PSORS1C1
1.000 6 31120157 intron variant G/A;C snv 4
rs3130560
PSORS1C1
1.000 6 31129676 intron variant T/A;G snv 8.2E-06; 0.74 4
rs3130942 1.000 6 31229516 upstream gene variant C/G;T snv 4
rs3130982
PSORS1C1 ; CDSN
1.000 6 31116298 synonymous variant G/C;T snv 0.56; 1.3E-02 4
rs3131018
POU5F1 ; PSORS1C3
1.000 6 31175805 intron variant A/C;G snv 4
rs3132551
CDSN ; PSORS1C1
1.000 6 31118105 non coding transcript exon variant A/G;T snv 4
rs3134783 1.000 6 31229486 upstream gene variant G/A;T snv 4
rs3778639
PSORS1C1
1.000 6 31125999 intron variant A/C;G;T snv 4
rs3823417
PSORS1C1
1.000 6 31133092 intron variant G/A;C;T snv 4
rs3828917
MICB
1.000 6 31498140 5 prime UTR variant G/A;T snv 4
rs386580036
CDSN ; PSORS1C1
1.000 6 31117492 synonymous variant A/G snv 4
rs386580037
PSORS1C1 ; CDSN
1.000 6 31117423 synonymous variant A/G snv 4
rs3869096
MUC22
1.000 6 31016627 intron variant T/A;G snv 4
rs4081552 1.000 6 31385912 upstream gene variant G/A;T snv 4
rs540151006
PSORS1C1 ; CDSN
1.000 6 31120802 intron variant A/G snv 4
rs541134362
PSORS1C1 ; CDSN
1.000 6 31118905 intron variant C/T snv 4
rs542420252
PSORS1C1
1.000 6 31133806 intron variant G/A snv 4