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: rs10852628
rs10852628
1 1.000 0.040 16 90013519 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs8059973
rs8059973
1 1.000 0.040 16 90013126 intron variant A/G snv 0.78 0.700 1.000 1 2012 2012