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: rs6271
rs6271
5 1.000 0.040 9 133657152 missense variant C/T snv 4.6E-02 4.8E-02 0.700 1.000 2 2016 2017