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: 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: rs2240395
rs2240395
TBXAS1
1 1.000 0.080 7 140018347 intron variant C/G;T snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs2523822
rs2523822 		1 1.000 0.080 6 29860883 intron variant A/G snv 0.26 0.800 1.000 1 2011 2011
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: 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: 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: 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: rs6694270
rs6694270 		1 1.000 0.080 1 18793883 intergenic variant A/G snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs72631567
rs72631567 		2 1.000 0.080 2 5092045 intergenic variant A/G snv 4.5E-02 0.700 1.000 1 2017 2017
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: rs73122578
rs73122578
ROBO1
1 1.000 0.080 3 79310483 intron variant A/C snv 0.27 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