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: rs7581030
rs7581030
1 1.000 0.120 2 71345325 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs7568069
rs7568069
2 1.000 0.120 2 71357355 intron variant G/A snv 0.48 0.010 1.000 1 2017 2017