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: rs13078828
rs13078828
LRIG1
1 3 66429063 intron variant G/A snv 2.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs2454138
rs2454138
HLA-DRB1
3 0.925 0.120 6 32602624 intergenic variant G/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs2681735
rs2681735
RGS6
1 14 72345817 intron variant A/G snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs2854275
rs2854275
HLA-DQB1 ; HLA-DQB1-AS1
4 0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs477515
rs477515
HLA-DRB1
10 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs522308
rs522308 		3 0.925 0.120 6 32614145 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6934608
rs6934608
F13A1 ; MIR5683 ; MIR7853
1 6 6169657 intron variant T/G snv 8.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs75727053
rs75727053 		1 20 38196318 regulatory region variant T/G snv 1.3E-02 0.700 1.000 1 2013 2013