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: rs112370447
rs112370447
1 1.000 0.040 7 107536335 intron variant C/T snv 0.27 0.700 1.000 1 2017 2017