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rs769399002

From SNPedia

ClinVar
Risk rs769399002(;)
Alt rs769399002(;)
Reference rs769399002(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene LAMB2 USP19
CLNDBN Nephrotic syndrome, type 5, with or without ocular abnormalities
Reversed 0
HGVS NC_000003.11:g.49159496delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000015637.27,