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: rs12997235
rs12997235
1 2 27006211 intron variant A/C snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs6705514
rs6705514
1 2 26991069 intron variant T/A;C;G snv 0.700 1.000 1 2018 2018