Related gene-specific medical variations for Gene (Select 23770) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3095343	NM_012181.5(FKBP8):c.766G>A (p.Ala256Thr)	FKBP8, LOC112543469 (A255T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095342	NM_012181.5(FKBP8):c.760T>A (p.Ser254Thr)	FKBP8, LOC112543469 (S253T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095341	NM_012181.5(FKBP8):c.614T>C (p.Val205Ala)	FKBP8, LOC112543469 (V204A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319725	NM_012181.5(FKBP8):c.632A>C (p.Glu211Ala)	FKBP8, LOC112543469 (E210A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255761	NM_012181.5(FKBP8):c.608C>T (p.Thr203Met)	FKBP8, LOC112543469 (T203M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 689698	NM_012181.5(FKBP8):c.724G>A (p.Ala242Thr)	FKBP8, LOC112543469 (A241T +1 more)	Single nucleotide variant (missense variant)	Marfanoid habitus and intellectual disability	GUncertain significance

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