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: rs61858823
rs61858823 		1 1.000 0.080 10 65095495 intergenic variant G/A snv 1.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs6582630
rs6582630 		1 1.000 0.080 12 38349706 intergenic variant G/A snv 0.62 0.800 1.000 1 2009 2009
dbSNP: rs72696020
rs72696020 		1 1.000 0.080 14 88105563 intergenic variant G/A snv 9.9E-03 0.700 1.000 1 2017 2017
dbSNP: rs2025009
rs2025009
RAD51B ; LOC107984679
1 1.000 0.080 14 68376888 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs28521457
rs28521457
LRBA
1 1.000 0.080 4 150759175 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs114577328
rs114577328
HLA-A
2 1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs597480
rs597480
SYTL2
1 1.000 0.080 11 85725825 missense variant G/C;T snv 0.59; 3.2E-05 0.700 1.000 1 2017 2017
dbSNP: rs3129900
rs3129900
TSBP1 ; TSBP1-AS1
3 0.882 0.200 6 32338202 intron variant G/T snv 0.83 0.800 1.000 1 2010 2010
dbSNP: rs116606120
rs116606120 		1 1.000 0.080 5 28665845 intron variant T/A snv 1.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs114811931
rs114811931 		1 1.000 0.080 5 161257724 intergenic variant T/C snv 1.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs6139258
rs6139258
RNF24
2 1.000 0.080 20 3977969 intron variant T/C snv 3.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs7828135
rs7828135
TPD52
1 1.000 0.080 8 80146584 intron variant T/C snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs2395029
rs2395029
HCP5
12 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 0.800 1.000 2 2009 2019