Source: ALL
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: rs4804217
rs4804217
PCP2
3 1.000 0.040 19 7634461 intron variant C/T snv 0.29 0.010 1.000 1 2018 2018