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: rs401681
rs401681
42 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.800 1.000 1 2010 2010
dbSNP: rs381949
rs381949
3 1.000 0.040 5 1322353 intron variant G/A snv 0.44 0.700 1.000 1 2018 2018