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: rs778360818
rs778360818
PLOD2
9 0.851 0.120 3 146079255 missense variant C/A snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs780770356
rs780770356
PLOD2 ; LNCSRLR
9 0.851 0.120 3 146071125 stop gained G/A snv 0.700 0