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: rs1422798
rs1422798
7 0.807 0.080 5 158893869 intron variant C/G snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs62385385
rs62385385
7 0.807 0.080 5 158940241 intron variant T/A snv 0.32 0.700 1.000 1 2016 2016