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: rs2925979
rs2925979
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.800 1.000 9 2010 2019
dbSNP: rs56823429
rs56823429
2 16 81500184 intron variant C/A;G;T snv 0.700 1.000 2 2015 2018