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: rs2609997
rs2609997
PENK ; LOC101929415
3 0.882 0.120 8 56447926 intron variant T/C snv 0.34 0.020 1.000 2 2012 2015