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: rs7561675
rs7561675
1 2 24024948 intron variant A/G snv 0.73 0.700 1.000 1 2016 2016
dbSNP: rs925228
rs925228
1 2 24023809 intron variant A/G snv 0.73 0.700 1.000 1 2016 2016