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: rs1060501198
rs1060501198
3 0.925 0.040 17 7674900 missense variant T/C;G snv 0.020 1.000 2 2006 2010
dbSNP: rs876658902
rs876658902
3 0.925 0.040 17 7676182 missense variant C/T snv 0.020 1.000 2 2006 2010