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: rs16899524
rs16899524
MICA-AS1
2 6 31394533 non coding transcript exon variant C/T snv 0.10 0.800 1.000 1 2013 2013
dbSNP: rs2023472
rs2023472
TRIM31 ; TRIM31-AS1
1 6 30108087 missense variant A/C;G snv 4.1E-06; 0.68 0.800 1.000 1 2013 2013
dbSNP: rs2523608
rs2523608
HLA-B ; MIR6891
6 0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19 0.800 1.000 1 2013 2013
dbSNP: rs2596466
rs2596466 		2 1.000 0.120 6 31437840 intron variant T/C snv 5.3E-02 0.800 1.000 1 2013 2013
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.800 1.000 1 2013 2013
dbSNP: rs9260489
rs9260489
HLA-A
2 1.000 0.080 6 29952555 upstream gene variant T/A;G snv 0.800 1.000 1 2013 2013
dbSNP: rs9264638
rs9264638
HLA-B ; HLA-C
1 6 31270541 intron variant G/A;C snv 0.800 1.000 1 2013 2013