Variants in gene PROM1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_006017.3(PROM1):c.103G>C (p.Glu35Gln)	rs200290535	0.00095
NM_006017.3(PROM1):c.134A>G (p.Asp45Gly)	rs201559220	0.00095
NM_006017.3(PROM1):c.1344C>T (p.Ile448=)	rs147174580	0.00005
NM_006017.3(PROM1):c.2374-14dup	rs370477050
NM_006017.3(PROM1):c.879C>T (p.Ser293=)	rs148242593

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