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: rs910869
rs910869
2 20 34704973 intron variant C/T snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs910870
rs910870
2 20 34705089 intron variant T/C snv 0.50 0.700 1.000 1 2010 2010