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: rs201831100
rs201831100
1 19 6804082 intron variant T/C snv 5.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs8106212
rs8106212
2 19 6802560 intron variant C/T snv 3.2E-02 0.700 1.000 1 2016 2016