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: rs20556
rs20556
LAMB1
1 1.000 0.040 7 107953544 missense variant T/C snv 0.65 0.66 0.010 1.000 1 2015 2015