List of variants in gene NDUFV1 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_007103.4(NDUFV1):c.511-290G>A	rs2514064	0.95327
NM_007103.4(NDUFV1):c.72+34T>C	rs1871043	0.45601
NM_007103.4(NDUFV1):c.327-36G>C	rs72932599	0.05977
NM_007103.4(NDUFV1):c.1056T>C (p.Ala352=)	rs11227859	0.05117
NM_007103.4(NDUFV1):c.549C>G (p.Gly183=)	rs10896187	0.05020
NM_007103.4(NDUFV1):c.511-94C>T	rs11227856	0.05017
NM_007103.4(NDUFV1):c.72+154G>A	rs11227853	0.05016
NM_007103.4(NDUFV1):c.326+278C>G	rs74344930	0.04774
NM_007103.4(NDUFV1):c.327-136C>A	rs73490571	0.03997
NM_007103.4(NDUFV1):c.511-65C>T	rs111907965	0.02486
NM_007103.4(NDUFV1):c.1080+39G>C	rs112015076	0.01805
NM_007103.4(NDUFV1):c.914-36C>G	rs2306144	0.00937
NM_007103.4(NDUFV1):c.150C>T (p.Asp50=)	rs11540012	0.00143
NM_007103.4(NDUFV1):c.72+15G>T	rs187400726	0.00109
NM_007103.4(NDUFV1):c.819C>T (p.Thr273=)	rs150859374	0.00093
NM_007103.4(NDUFV1):c.597C>T (p.Arg199=)	rs151104852	0.00087
NM_007103.4(NDUFV1):c.366G>A (p.Pro122=)	rs140445386	0.00083
NM_007103.4(NDUFV1):c.348C>T (p.Asn116=)	rs139824241	0.00047
NM_007103.4(NDUFV1):c.700+12C>T	rs200417926	0.00020
NM_007103.4(NDUFV1):c.511-34_511-24del	rs111437532
NM_007103.4(NDUFV1):c.700+188T>G	rs3016861
NM_007103.4(NDUFV1):c.701-20C>G	rs371709474
NM_007103.4(NDUFV1):c.73-158dup	rs11413867
NM_007103.4(NDUFV1):c.73-159_73-158dup	rs11413867
NM_007103.4(NDUFV1):c.73-213G>A	rs111396223
NM_007103.4(NDUFV1):c.913+29G>T	rs11227858

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