Variants in gene POR 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_001395413.1(POR):c.1499C>T (p.Ala500Val)	rs1057868	0.26722
NM_001395413.1(POR):c.360C>T (p.Ala120=)	rs41299490	0.00719
NM_001395413.1(POR):c.508-4G>A	rs41299496	0.00462
NM_001395413.1(POR):c.633-5C>G	rs72555509	0.00047
NM_001395413.1(POR):c.1227C>T (p.Ser409=)	rs41301424	0.00041
NM_001395413.1(POR):c.1806+8G>A	rs72557952	0.00024

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