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: rs10474352
rs10474352
2 0.925 0.080 5 91436408 intron variant C/T snv 0.23 0.710 1.000 2 2014 2017
dbSNP: rs332529
rs332529
1 1.000 0.080 5 91493653 intron variant G/A;T snv 0.700 1.000 1 2017 2017