"PreventionGenetics, part of Exact Sciences"[submitter] AND "LIN7B"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1279757	NM_022165.3(LIN7B):c.37+8T>C	LIN7B, LOC130064901	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3046227	NM_022165.3(LIN7B):c.180G>T (p.Thr60=)	LIN7B	Single nucleotide variant (synonymous variant)	LIN7B-related disorder	GLikely benign
Select item 3051036	NM_022165.3(LIN7B):c.201C>A (p.Ala67=)	LIN7B	Single nucleotide variant (synonymous variant)	LIN7B-related disorder	GLikely benign

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