Related gene-specific medical variations for Gene (Select 151827) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2525352	NM_001172779.2(LRRC34):c.77G>A (p.Arg26Lys)	LRRC34, LOC129937874 (R26K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307817	NM_001172779.2(LRRC34):c.110C>G (p.Thr37Ser)	LOC129937874, LRRC34 (T37S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance