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: rs10206196
rs10206196
1 2 24914454 intron variant T/C snv 0.55 0.700 1.000 1 2016 2016
dbSNP: rs35609705
rs35609705
1 2 24868853 intron variant AA/-;A;AAA;AAAA delins 0.700 1.000 1 2016 2016