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: rs11653357
rs11653357
2 17 35596588 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs533229216
rs533229216
1 17 35658446 intron variant C/T snv 1.8E-03 0.700 1.000 1 2016 2016