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rs797044907

From SNPedia

ClinVar
Risk rs797044907(AGCT;AGCT)
Alt rs797044907(AGCT;AGCT)
Reference rs797044907(;)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene LRTOMT
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.71819708_71819709insAGCT
CLNSRC
CLNACC RCV000190734.1,