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: rs6142206
rs6142206
2 20 34624251 intron variant G/A snv 0.30 0.700 1.000 1 2010 2010
dbSNP: rs764598
rs764598
2 20 34573346 intron variant C/G snv 4.7E-02 0.700 1.000 1 2010 2010