ClinVar (all) for Orgtrack (Select 508721) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2135980	NC_000011.10:g.636784T>G		Single nucleotide variant	methamphetamine use disorder	GUncertain risk allele
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	NC_000006.12:g.35702206A>G	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
Select item 256786	NM_000754.4(COMT):c.408C>G (p.Leu136=)	COMT	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

ClinVar