Variants in gene SURF1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_003172.4(SURF1):c.573C>G (p.Thr191=)	rs28715079	0.05492
NM_003172.4(SURF1):c.280T>C (p.Leu94=)	rs28615629	0.04975
NM_003172.4(SURF1):c.167C>G (p.Ala56Gly)	rs116779216	0.01318
NM_003172.4(SURF1):c.543C>T (p.Phe181=)	rs62637580	0.01036
NM_003172.4(SURF1):c.604G>C (p.Asp202His)	rs72619327	0.00517
NM_003172.4(SURF1):c.883C>T (p.Arg295Cys)	rs147312193	0.00385

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