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rs797044884

From SNPedia

ClinVar
Risk rs797044884(AG;AG)
Alt rs797044884(AG;AG)
Reference rs797044884(;)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CLTC
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000017.10:g.57754490_57754491dupGA
CLNSRC
CLNACC RCV000190705.1,