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: rs78900282
rs78900282
1 6 87568337 intron variant C/T snv 7.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs9342115
rs9342115
1 6 87556101 intron variant T/C snv 7.7E-02 0.700 1.000 1 2018 2018