List of variants in gene ADGRV1 reported as uncertain significance for Hearing impairment

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_032119.4(ADGRV1):c.2636C>T (p.Thr879Met)	rs201007778	0.00014
NM_032119.4(ADGRV1):c.12208G>A (p.Val4070Ile)	rs200943280	0.00005
NM_032119.4(ADGRV1):c.8110A>T (p.Ile2704Phe)	rs376318779	0.00005
NM_032119.4(ADGRV1):c.11783A>G (p.Tyr3928Cys)	rs1179343056	0.00003
NM_032119.4(ADGRV1):c.3245C>T (p.Pro1082Leu)	rs768921869	0.00002
NM_032119.4(ADGRV1):c.5969T>C (p.Val1990Ala)	rs376559614	0.00002
NM_032119.4(ADGRV1):c.14474A>G (p.Asp4825Gly)	rs377619015	0.00001
NM_032119.4(ADGRV1):c.16625C>A (p.Ala5542Asp)	rs373121319	0.00001
NM_032119.4(ADGRV1):c.7735G>A (p.Val2579Met)	rs755818826	0.00001
NM_032119.4(ADGRV1):c.17333T>C (p.Leu5778Pro)	rs2150406842
NM_032119.4(ADGRV1):c.1954A>G (p.Ile652Val)	rs749308308
NM_032119.4(ADGRV1):c.3232G>A (p.Glu1078Lys)	rs2149447085
NM_032119.4(ADGRV1):c.6274A>C (p.Ile2092Leu)	rs2149586553
NM_032119.4(ADGRV1):c.7319C>T (p.Ala2440Val)	rs2149640041
NM_032119.4(ADGRV1):c.9512T>C (p.Leu3171Ser)	rs2149767008

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