Variants in gene SPG7 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 16

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HGVS	dbSNP	gnomAD frequency
NM_003119.4(SPG7):c.1507A>G (p.Thr503Ala)	rs2292954	0.12849
NM_003119.4(SPG7):c.2063G>A (p.Arg688Gln)	rs12960	0.12801
NM_003119.4(SPG7):c.1664-15C>A	rs80292600	0.01888
NM_003119.4(SPG7):c.2188A>G (p.Asn730Asp)	rs35749032	0.01431
NM_003119.4(SPG7):c.2295C>T (p.Asp765=)	rs61747712	0.01110
NM_003119.4(SPG7):c.2280G>A (p.Pro760=)	rs11559075	0.01053
NM_003119.4(SPG7):c.1936+12C>T	rs112379588	0.00628
NM_003119.4(SPG7):c.1937-16C>G	rs74590011	0.00558
NM_003119.4(SPG7):c.1457G>A (p.Arg486Gln)	rs111475461	0.00551
NM_003119.4(SPG7):c.1032C>T (p.Gly344=)	rs116319889	0.00450
NM_003119.4(SPG7):c.987+19G>A	rs62071462	0.00263
NM_003119.4(SPG7):c.1324+4187C>T	rs143254053	0.00185
NM_003119.4(SPG7):c.1083G>A (p.Ala361=)	rs114135540	0.00089
NM_003119.4(SPG7):c.1324+10C>T	rs202070075	0.00073
NM_003119.4(SPG7):c.199C>T (p.Leu67=)	rs148315471	0.00066
NM_003119.4(SPG7):c.1422C>T (p.His474=)	rs201482100	0.00004

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