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: rs773850151
rs773850151
2 1.000 6 98899353 missense variant C/G;T snv 8.0E-06 0.700 1.000 2 2015 2017