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: rs370989584
rs370989584 		1 1.000 0.080 4 133040031 intergenic variant T/- del 8.8E-03 0.700 1.000 1 2018 2018
dbSNP: rs376674848
rs376674848 		1 1.000 0.080 12 84220725 intron variant -/ATGTGT delins 0.700 1.000 1 2018 2018
dbSNP: rs4052756
rs4052756 		1 1.000 0.080 6 19914263 intergenic variant C/T snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs4239217
rs4239217
HNF1B
1 1.000 0.080 17 37738996 intron variant A/G snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs4607001
rs4607001
LOC105372562 ; LOC105372563
1 1.000 0.080 20 22467899 intron variant C/T snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs529138199
rs529138199
NCAM2
1 1.000 0.080 21 21005810 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs561726060
rs561726060
LOC105372018
1 1.000 0.080 18 22263993 regulatory region variant C/T snv 4.4E-03 0.700 1.000 1 2018 2018
dbSNP: rs571866661
rs571866661 		1 1.000 0.080 11 77315297 downstream gene variant TTTTTTTTTTTTTTTTT/-;T;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT delins 8.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs6064391
rs6064391
CSTF1
1 1.000 0.080 20 56396330 intron variant G/T snv 0.44 0.010 1.000 1 2015 2015
dbSNP: rs60856912
rs60856912
BPTF
1 1.000 0.080 17 67896227 intron variant G/T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs6149499
rs6149499
LOC101929006 ; LOC105375005
1 1.000 0.080 6 29288284 intron variant AT/-;ATAT;ATATAT;ATATATCATGTATATATATATATAT;ATATCATGTATATATATATATAT delins 0.700 1.000 1 2018 2018
dbSNP: rs6499199
rs6499199
CDH1
1 1.000 0.080 16 68815934 intron variant C/T snv 0.14 0.010 1.000 1 2018 2018
dbSNP: rs757209
rs757209
HNF1B
1 1.000 0.080 17 37742842 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs757211
rs757211
HNF1B
1 1.000 0.080 17 37736488 intron variant T/C snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs76165228
rs76165228
PPP1R14C
1 1.000 0.080 6 150198039 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs79024726
rs79024726
CSMD2
1 1.000 0.080 1 33832760 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs7981863
rs7981863 		1 1.000 0.080 13 73238004 intergenic variant C/T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs8067269
rs8067269
BRCA1
1 1.000 0.080 17 43083782 intron variant G/A snv 0.52 0.010 1.000 1 2015 2015
dbSNP: rs8176199
rs8176199
BRCA1
1 1.000 0.080 17 43078507 intron variant T/G snv 0.23 0.010 1.000 1 2015 2015
dbSNP: rs8176323
rs8176323 		1 1.000 0.080 17 43043694 downstream gene variant G/C snv 0.31 0.010 1.000 1 2015 2015
dbSNP: rs819913
rs819913
PLPPR4
1 1.000 0.080 1 99299799 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs872267
rs872267
EEFSEC
1 1.000 0.080 3 128169224 intron variant G/A snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs882380
rs882380
SKAP1
1 1.000 0.080 17 48216874 intron variant C/A snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs911162
rs911162
CSTF1 ; AURKA
1 1.000 0.080 20 56391393 intron variant A/C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs9600103
rs9600103 		1 1.000 0.080 13 73237742 intergenic variant A/T snv 0.33 0.700 1.000 1 2016 2016