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: rs4141194
rs4141194
1 11 16989629 intron variant C/A snv 0.20 0.700 1.000 3 2018 2018
dbSNP: rs11024102
rs11024102
7 0.851 0.040 11 16987058 intron variant T/C snv 0.20 0.700 1.000 1 2018 2018