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: rs16836697
rs16836697
1 4 5137397 intron variant C/T snv 7.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs6817353
rs6817353
1 4 5239844 intron variant A/G snv 0.25 0.700 1.000 1 2013 2013