Variants with conflicting interpretations "uncertain significance" from Undiagnosed Diseases Network, NIH and "likely 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000304.4(PMP22):c.353C>T (p.Thr118Met)	rs104894619	0.00378
NM_022168.4(IFIH1):c.1879G>T (p.Glu627Ter)	rs35744605	0.00367
NM_000540.3(RYR1):c.11798A>G (p.Tyr3933Cys)	rs147136339	0.00108
NM_000540.3(RYR1):c.4711A>G (p.Ile1571Val)	rs146429605	0.00107
NM_022168.4(IFIH1):c.1066C>A (p.Pro356Thr)	rs150317197	0.00078
NM_000540.3(RYR1):c.10097G>A (p.Arg3366His)	rs137932199	0.00073
NM_001243133.2(NLRP3):c.2176A>G (p.Ser726Gly)	rs147946775	0.00049
NM_001022.4(RPS19):c.164C>T (p.Thr55Met)	rs147508369	0.00039
NM_000089.4(COL1A2):c.2425C>T (p.Pro809Ser)	rs145355907	0.00032
NM_001606.5(ABCA2):c.1193C>A (p.Thr398Lys)	rs143473036
Single allele

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