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: rs868408509
rs868408509
LAMA2
6 0.827 0.160 6 128883315 missense variant C/G;T snv 4.6E-06 0.010 1.000 1 2015 2015