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: rs11783023
rs11783023
1 1.000 0.040 8 140629163 intron variant C/T snv 0.70 0.700 1.000 1 2019 2019