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: rs2555592
rs2555592
2 13 33202766 intron variant T/G snv 4.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs2764627
rs2764627
2 0.925 0.040 13 33202941 intron variant C/T snv 5.0E-02 0.700 1.000 1 2012 2012