Variants in gene HOGA1 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_138413.4(HOGA1):c.212-21A>G	rs11817730	0.19877
NM_138413.4(HOGA1):c.700+67G>A	rs2297643	0.16278
NM_138413.4(HOGA1):c.708G>T (p.Val236=)	rs61731946	0.00068
NM_138413.4(HOGA1):c.931C>T (p.Pro311Ser)	rs116455504	0.00047
NM_138413.4(HOGA1):c.237C>T (p.Gly79=)	rs148094180	0.00044
NM_138413.4(HOGA1):c.185A>T (p.His62Leu)	rs150812556	0.00030
NM_138413.4(HOGA1):c.554C>T (p.Thr185Met)	rs115282699	0.00019
NM_138413.4(HOGA1):c.828C>T (p.Asn276=)	rs201683794	0.00006
NM_138413.4(HOGA1):c.720C>T (p.Cys240=)	rs183301169	0.00004
NM_138413.4(HOGA1):c.294G>A (p.Gln98=)	rs777208958	0.00001

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