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: rs13243553
rs13243553
1 7 133822202 intron variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs7804463
rs7804463
1 7 133762898 intron variant T/C snv 0.47 0.700 1.000 1 2018 2018