Related gene-specific medical variations for Gene (Select 100874080) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3092870	NM_005766.4(FARP1):c.2244T>G (p.Ile748Met)	FARP1, FARP1-AS1 (I748M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2643885	NM_005766.4(FARP1):c.2163G>T (p.Thr721=)	FARP1, FARP1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2287720	NM_005766.4(FARP1):c.2152G>C (p.Ala718Pro)	FARP1, FARP1-AS1 (A718P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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