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: rs112815007
rs112815007 		1 20 551613 intergenic variant A/G snv 3.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs114965806
rs114965806 		1 5 36406285 intergenic variant C/T snv 2.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs144261420
rs144261420
CDC42EP3 ; LOC105374465
1 2 37727574 intron variant A/G snv 8.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs61134957
rs61134957 		1 8 91586775 intron variant A/C snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs62324204
rs62324204
IL21-AS1
1 4 122626441 non coding transcript exon variant T/C snv 6.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs62480124
rs62480124
CSMD1
1 8 3921114 intron variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7211029
rs7211029
RBFOX3
1 17 79145226 intron variant C/T snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs74448913
rs74448913
CSNK2A1
1 20 527787 intron variant T/A snv 3.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs77942316
rs77942316
SLC26A7
1 8 91347109 intron variant G/A snv 3.0E-02 0.700 1.000 1 2016 2016