Variants in gene DYNC1H1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.10016G>A (p.Arg3339His)	rs2152591288
NM_001376.5(DYNC1H1):c.10030C>T (p.Arg3344Trp)	rs2048519381
NM_001376.5(DYNC1H1):c.1792C>T (p.Arg598Cys)	rs587780564
NM_001376.5(DYNC1H1):c.2327C>T (p.Pro776Leu)	rs1057518083
NM_001376.5(DYNC1H1):c.3278T>C (p.Phe1093Ser)	rs1555408829
NM_001376.5(DYNC1H1):c.4868G>A (p.Arg1623Gln)	rs1064796765
NM_001376.5(DYNC1H1):c.6994C>T (p.Arg2332Cys)	rs1057518961
NM_001376.5(DYNC1H1):c.752G>A (p.Arg251His)	rs794727634
NM_001376.5(DYNC1H1):c.791G>A (p.Arg264Gln)	rs713993043
NM_001376.5(DYNC1H1):c.874C>T (p.Arg292Trp)	rs2047850664
NM_001376.5(DYNC1H1):c.917A>G (p.His306Arg)	rs387906738

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