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: rs10764338
rs10764338
1 1.000 10 22577963 intron variant T/C snv 0.82 0.010 1.000 1 2015 2015
dbSNP: rs10828317
rs10828317
9 0.776 0.280 10 22550699 missense variant T/C snv 0.010 1.000 1 2013 2013