Source: GWASCAT ×
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: rs10411970
rs10411970 		1 1.000 0.040 19 4814636 downstream gene variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11204668
rs11204668
ADAMTSL4-AS1
1 1.000 0.040 1 150571210 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs11757201
rs11757201 		5 0.851 0.040 6 137682685 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1545536
rs1545536
GSDMD
1 1.000 0.040 8 143560999 splice region variant C/A;G;T snv 4.0E-06; 0.26 0.700 1.000 1 2019 2019
dbSNP: rs17552787
rs17552787 		1 1.000 0.040 7 50264486 upstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2074478
rs2074478
PSORS1C1 ; PSORS1C2
1 1.000 0.040 6 31137856 3 prime UTR variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2305742
rs2305742
IL12RB1
1 1.000 0.040 19 18080631 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2516392
rs2516392
LTA ; LOC100287329
1 1.000 0.040 6 31561557 downstream gene variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2523589
rs2523589 		1 0.851 0.200 6 31359557 upstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2759663
rs2759663
CRB1
2 0.925 0.080 1 197415296 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2914119
rs2914119
LINC01100 ; IL12A-AS1
1 1.000 0.040 3 160026651 non coding transcript exon variant C/G;T snv 0.73 0.700 1.000 1 2019 2019
dbSNP: rs3135461
rs3135461 		1 1.000 0.040 6 32712345 regulatory region variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs34390431
rs34390431
LINC02009
1 1.000 0.040 3 46423449 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs35268627
rs35268627 		1 1.000 0.040 1 247400588 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs3746181
rs3746181
PGPEP1
1 1.000 0.040 19 18366207 3 prime UTR variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs3813961
rs3813961
MAPKAPK2
1 1.000 0.040 1 206732454 3 prime UTR variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs3869097
rs3869097
MUC22
1 1.000 0.040 6 31016693 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs41546314
rs41546314
HLA-A
1 1.000 0.040 6 29942601 synonymous variant C/T snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs4466418
rs4466418
NSMCE2
1 1.000 0.040 8 125311545 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4493469
rs4493469
LOC105377067
1 1.000 0.040 3 46136500 intergenic variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs4699030
rs4699030
NFKB1
1 1.000 0.040 4 102582667 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs4845140
rs4845140
IL19
1 1.000 0.040 1 206797125 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6805758
rs6805758
IL12A-AS1
1 1.000 0.040 3 159927882 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs7193275
rs7193275 		1 1.000 0.040 16 85984869 non coding transcript exon variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs76830965
rs76830965
IL12A-AS1
2 0.925 0.120 3 159919889 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019