"WangQJ Lab, Chinese People's Liberation Army General Hospital"[submit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1185091	NM_001038603.3(MARVELD2):c.1122dup (p.Arg375Ter)	MARVELD2 (R375*)	Duplication (nonsense)	Autosomal recessive nonsyndromic hearing loss 49	GLikely pathogenic
Select item 1185092	NM_001038603.3(MARVELD2):c.1208_1211del (p.Arg403fs)	MARVELD2 (R391fs +1 more)	Microsatellite (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 49	GLikely pathogenic