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: rs7554511
rs7554511
3 0.925 0.040 1 200908434 intron variant C/A snv 0.22 0.810 1.000 3 2012 2017
dbSNP: rs35730213
rs35730213
1 1 200905101 intron variant G/C snv 0.22 0.700 1.000 1 2015 2015