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: rs6795735
rs6795735
7 0.882 0.120 3 64719689 intron variant C/A;G;T snv 0.820 1.000 3 2013 2019
dbSNP: rs62247658
rs62247658
4 0.851 0.040 3 64729479 intron variant C/T snv 0.42 0.700 1.000 1 2016 2016