rs793888525, ADGRG6

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
LETHAL CONGENITAL CONTRACTURE SYNDROME 9
3 0.925 0.080 6 142408187 missense variant T/A snv 0.800 0
Arthrogryposis
CUI: C0003886
Disease: Arthrogryposis
33 0.925 0.080 6 142408187 missense variant T/A snv 0.700 0