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: rs2302515
rs2302515
1 1.000 0.040 12 7652640 missense variant C/G snv 0.78 0.76 0.010 1.000 1 2017 2017