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: rs7756992
rs7756992
12 0.827 0.240 6 20679478 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9368222
rs9368222
8 1.000 0.080 6 20686765 intron variant C/A;T snv 0.700 1.000 1 2012 2012