C4540024[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 982616	NM_001145026.2(PTPRQ):c.3G>A (p.Met1Ile)	PTPRQ (M1I)	Single nucleotide variant (missense variant +1 more)	Hearing loss, autosomal dominant 73	GLikely pathogenic
Select item 1285598	NM_001145026.2(PTPRQ):c.5606A>G (p.Gln1869Arg)	PTPRQ (Q1869R)	Single nucleotide variant (missense variant)	Hearing loss, autosomal dominant 73	GUncertain significance