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: rs16834898
rs16834898
2 0.925 0.080 2 192772562 intron variant A/C snv 0.53 0.010 1.000 1 2013 2013
dbSNP: rs6434568
rs6434568
2 0.925 0.080 2 192758626 intron variant C/A;T snv 0.010 1.000 1 2013 2013