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rs794728135

From SNPedia

ClinVar
Risk rs794728135(;)
Alt rs794728135(;)
Reference rs794728135(GCTTGATGC;GCTTGATGC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7556023_7556031delCTTGATGCG
CLNSRC
CLNACC RCV000181356.2,