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rs797044691

From SNPedia

ClinVar
Risk rs797044691(A;A)
Alt rs797044691(A;A)
Reference rs797044691(;)
Significance Probable-Pathogenic
Disease Microcephaly
Variation info
Gene RTTN
CLNDBN Microcephaly, short stature, and polymicrogyria with or without seizures
Reversed 1
HGVS NC_000018.9:g.67794741dupT
CLNSRC
CLNACC RCV000176596.1,