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: rs3817334
rs3817334
7 1.000 0.080 11 47629441 intron variant C/T snv 0.36 0.700 1.000 1 2017 2017