ClinVar for MedGen (Select 339856) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3252039	Multiple alleles	FAAH, LOC129930482 (P129T)	Single nucleotide variant (missense variant)	PAIN SENSITIVITY QUANTITATIVE TRAIT LOCUS 1	GAffects
Select item 3065619	NM_001441.3(FAAH):c.549del (p.His184fs)	FAAH (H184fs)	Deletion (frameshift variant)	Polysubstance abuse, susceptibility to	GLikely pathogenic
Select item 6724	NM_001441.3(FAAH):c.385C>A (p.Pro129Thr)	FAAH (P129T)	Single nucleotide variant (missense variant)	Polysubstance abuse, susceptibility to +1 more	GBenign/Likely benign

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