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: rs11014271
rs11014271
1 10 24871573 intron variant C/T snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs7394259
rs7394259
1 10 24877899 intron variant G/A snv 0.12 0.700 1.000 1 2018 2018