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: rs741013
rs741013
1 3 64306961 intron variant A/T snv 6.0E-02 0.800 1.000 1 2013 2013
dbSNP: rs17404667
rs17404667
1 3 64288876 intron variant C/G snv 6.2E-02 0.700 1.000 1 2013 2013