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: rs11188501
rs11188501
1 10 95841162 intron variant G/A snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs4918970
rs4918970
1 10 95803250 intron variant G/A snv 0.27 0.700 1.000 1 2018 2018