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: rs10994318
rs10994318
2 0.925 0.040 10 60366098 intron variant G/C snv 7.3E-02 0.700 1.000 1 2019 2019