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rs766771165

From SNPedia

ClinVar
Risk rs766771165(A;A)
Alt rs766771165(A;A)
Reference rs766771165(;)
Significance Pathogenic
Disease not provided
Variation info
Gene AARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.44275018dupA
CLNSRC
CLNACC RCV000199735.1,