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: rs77969132
rs77969132
9 0.790 0.080 12 31441879 intron variant C/T snv 6.5E-04 0.700 1.000 1 2019 2019