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: rs78707713
rs78707713
2 1.000 0.120 10 69485520 intron variant T/C snv 8.5E-02 0.710 0.800 5 2015 2020
dbSNP: rs17490626
rs17490626
5 0.882 0.120 10 69458890 intron variant G/C snv 8.4E-02 0.700 1.000 1 2016 2016