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: rs932764
rs932764
6 10 94136183 intron variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9663362
rs9663362
1 10 94135420 intron variant G/A;C snv 0.700 1.000 1 2011 2011