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: rs627634
rs627634
1 15 48587094 intron variant C/T snv 7.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs686861
rs686861
2 15 48592808 intron variant A/G snv 9.1E-02 0.700 1.000 1 2018 2018