Related gene-specific medical variations for Gene (Select 2289) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2338089	NM_004117.4(FKBP5):c.746G>A (p.Ser249Asn)	FKBP5, LOC129389497 (S249N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1702947	NM_004117.4(FKBP5):c.-19-3406A>G	FKBP5	Single nucleotide variant (intron variant)	Susceptibility to severe depressive disorder	GLikely risk allele
Select item 1702946	NM_004117.4(FKBP5):c.-20+13518C>T	FKBP5	Single nucleotide variant (intron variant)	Susceptibility to severe depressive disorder	GLikely risk allele
Select item 1702945	NM_004117.4(FKBP5):c.509-10306C>T	FKBP5	Single nucleotide variant (intron variant)	Susceptibility to severe depressive disorder	GLikely risk allele
Select item 1702944	NM_004117.4(FKBP5):c.-19-22418C>G	FKBP5	Single nucleotide variant (intron variant)	Susceptibility to severe depressive disorder	GLikely risk allele
Select item 1702943	NM_001145775.3(FKBP5):c.-20+18122T>C	FKBP5	Single nucleotide variant (intron variant)	Susceptibility to severe depressive disorder	GLikely risk allele
Select item 1702942	NM_004117.4(FKBP5):c.508+7498T>G	FKBP5	Single nucleotide variant (intron variant)	Susceptibility to severe depressive disorder	GLikely risk allele

ClinVar