Variants in gene CACNA1A with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.1499C>T (p.Thr500Met)	rs121908240	0.00001
NM_001127222.2(CACNA1A):c.2026G>A (p.Gly676Arg)	rs2144980758
NM_001127222.2(CACNA1A):c.4064C>T (p.Thr1355Ile)	rs2056767062
NM_001127222.2(CACNA1A):c.4927G>A (p.Asp1643Asn)	rs1064795531
NM_001127222.2(CACNA1A):c.526G>A (p.Val176Met)	rs1057521920
NM_001127222.2(CACNA1A):c.889G>A (p.Gly297Arg)	rs1168625480

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