Related gene-specific medical variations for Gene (Select 54602) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2376635	NM_019080.3(NDFIP2):c.16A>T (p.Ser6Cys)	NDFIP2, NDFIP2-AS1 (S6C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2206578	NM_019080.3(NDFIP2):c.11G>A (p.Arg4Gln)	NDFIP2, NDFIP2-AS1 (R4Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance