Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3117098
rs3117098
HCG23 ; TSBP1-AS1
4 0.851 0.280 6 32390736 non coding transcript exon variant G/A snv 0.72 0.810 1.000 1 2011 2020
dbSNP: rs404860
rs404860
NOTCH4
2 0.925 0.160 6 32216568 non coding transcript exon variant T/C snv 0.21 0.810 1.000 1 2011 2011
dbSNP: rs7130588
rs7130588 		3 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 0.810 1.000 1 2011 2011
dbSNP: rs7775228
rs7775228 		5 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 0.810 0.500 1 2011 2020
dbSNP: rs9268516
rs9268516 		3 0.882 0.200 6 32411712 upstream gene variant C/T snv 0.24 0.810 1.000 1 2012 2012
dbSNP: rs9272346
rs9272346
HLA-DQA1
6 0.790 0.320 6 32636595 intron variant G/A snv 0.54 0.810 1.000 1 2012 2019
dbSNP: rs987870
rs987870
HLA-DPA1 ; HLA-DPB1
3 0.851 0.160 6 33075103 intron variant A/G snv 0.19 0.810 1.000 1 2011 2011
dbSNP: rs992969
rs992969 		2 0.882 0.080 9 6209697 intergenic variant A/G;T snv 0.810 1.000 1 2010 2019
dbSNP: rs1588265
rs1588265
PDE4D
1 1.000 0.080 5 60073967 intron variant A/G;T snv 0.800 1.000 3 2009 2011
dbSNP: rs2073643
rs2073643
SLC22A5
4 1.000 0.080 5 132387596 intron variant T/C snv 0.46 0.800 1.000 3 2010 2012
dbSNP: rs1008723
rs1008723
GSDMB
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.800 1.000 1 2011 2019
dbSNP: rs10508372
rs10508372 		1 1.000 0.080 10 8930055 intergenic variant G/A snv 0.14 0.800 1.000 1 2011 2011
dbSNP: rs1101999
rs1101999
PYHIN1
1 1.000 0.080 1 158962765 intron variant C/T snv 0.92 0.800 1.000 1 2011 2011
dbSNP: rs11214966
rs11214966
LOC101928940
1 1.000 0.080 11 114360533 intron variant T/C snv 0.13 0.800 1.000 1 2011 2011
dbSNP: rs1701704
rs1701704
IKZF4 ; LOC105369781
5 0.851 0.200 12 56018703 intron variant T/G snv 0.25 0.800 1.000 1 2011 2011
dbSNP: rs17843604
rs17843604
HLA-DQA1
2 0.925 0.120 6 32652506 intergenic variant C/T snv 0.49 0.800 1.000 1 2010 2019
dbSNP: rs204993
rs204993
PBX2
3 0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 0.800 1.000 1 2011 2011
dbSNP: rs2069408
rs2069408
CDK2 ; PMEL
2 0.925 0.200 12 55970537 intron variant A/G snv 0.24 0.800 1.000 1 2011 2011
dbSNP: rs2305479
rs2305479
GSDMB
4 0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 0.800 1.000 1 2011 2018
dbSNP: rs2381416
rs2381416 		2 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 0.800 1.000 1 2011 2011
dbSNP: rs3019885
rs3019885
SLC30A8
2 0.925 0.120 8 117013406 intron variant T/A;G snv 0.800 1.000 1 2011 2011
dbSNP: rs3129890
rs3129890 		5 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs3129943
rs3129943
TSBP1 ; TSBP1-AS1
4 0.851 0.240 6 32370918 intron variant A/G snv 0.26 0.800 1.000 1 2011 2011
dbSNP: rs3763309
rs3763309
BTNL2 ; TSBP1-AS1
3 0.882 0.160 6 32408196 upstream gene variant C/A;T snv 0.800 1.000 1 2011 2018
dbSNP: rs3805236
rs3805236
GAB1
1 1.000 0.080 4 143436584 intron variant A/G snv 0.74 0.800 1.000 1 2011 2011