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: rs16948101
rs16948101
1 15 64604099 intron variant A/G snv 9.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs34059679
rs34059679
1 15 64663275 intron variant G/A snv 8.3E-02 0.700 1.000 1 2018 2018