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: rs1244793237
rs1244793237
GCA
1 1.000 0.120 2 162347645 missense variant C/G snv 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs748685566
rs748685566
GCA
1 1.000 0.120 2 162347642 missense variant C/G snv 4.0E-06 0.010 1.000 1 2011 2011