Source: ALL
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: rs1233491
rs1233491 		2 0.925 0.080 6 29493953 upstream gene variant G/C snv 5.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs2187668
rs2187668
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
20 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2015 2015
dbSNP: rs3094067
rs3094067
TRIM39 ; RPP21 ; TRIM39-RPP21
1 1.000 0.040 6 30331468 intron variant T/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs3094084
rs3094084 		1 1.000 0.040 6 30979732 upstream gene variant A/T snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs3130564
rs3130564
PSORS1C1
7 0.790 0.360 6 31133897 intron variant C/T snv 0.14 0.700 1.000 1 2015 2015
dbSNP: rs3131060
rs3131060 		1 1.000 0.040 6 30795514 downstream gene variant G/A snv 8.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs9267531
rs9267531
CSNK2B ; LY6G5B
3 0.882 0.120 6 31668965 non coding transcript exon variant A/G snv 7.5E-02 0.700 1.000 1 2015 2015