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: rs1940973
rs1940973
1 18 12550748 intron variant T/C snv 8.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs9959145
rs9959145
1 18 12606464 intron variant G/A;T snv 0.700 1.000 1 2012 2012