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: rs1741640
rs1741640
10 0.776 0.080 20 62357358 intron variant T/C snv 0.66 0.700 1.000 2 2019 2019
dbSNP: rs4925386
rs4925386
14 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010