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: rs77757620
rs77757620
2 1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 0.700 1.000 1 2017 2017