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: rs12526480
rs12526480
2 6 25533306 intron variant T/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs34164888
rs34164888
1 6 25521693 intron variant C/A;T snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs6913974
rs6913974
1 6 25528322 intron variant G/A snv 0.43 0.700 1.000 1 2016 2016