Variants with conflicting interpretations "uncertain significance" from Undiagnosed Diseases Network, NIH and "benign" from any submitter

Minimum review status of the submission from Undiagnosed Diseases Network, NIH:		Collection method of the submission from Undiagnosed Diseases Network, NIH:
Minimum review status of the other submission:		Collection method of the other submission:
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_015602.4(TOR1AIP1):c.554-4G>A	rs2245425	0.58997
NM_000304.4(PMP22):c.353C>T (p.Thr118Met)	rs104894619	0.00378
NM_000540.3(RYR1):c.4711A>G (p.Ile1571Val)	rs146429605	0.00107
NM_000540.3(RYR1):c.10097G>A (p.Arg3366His)	rs137932199	0.00073
Single allele

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