List of variants in gene NDUFS6 reported as likely pathogenic for not provided

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004553.6(NDUFS6):c.247C>T (p.Arg83Trp)	rs863224110	0.00003
NM_004553.6(NDUFS6):c.32_33dup (p.Asn12Ter)	rs769666581	0.00001
NM_004553.6(NDUFS6):c.132+1G>C
NM_004553.6(NDUFS6):c.187-1G>C
NM_004553.6(NDUFS6):c.187-2A>G
NM_004553.6(NDUFS6):c.288_292del (p.His96fs)	rs2111362314
NM_004553.6(NDUFS6):c.305A>T (p.Asn102Ile)	rs863224111
NM_004553.6(NDUFS6):c.335dup (p.Cys112fs)	rs2111364865
NM_004553.6(NDUFS6):c.344G>A (p.Cys115Tyr)	rs267606913

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