Variants in gene SPTA1 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely 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_003126.4(SPTA1):c.6531-12C>T	rs28525570	0.25447
NM_003126.4(SPTA1):c.620T>C (p.Leu207Pro)	rs121918643	0.00019
NM_003126.4(SPTA1):c.781T>C (p.Ser261Pro)	rs121918636	0.00003
NM_003126.4(SPTA1):c.101G>C (p.Arg34Pro)	rs567686069
NM_003126.4(SPTA1):c.1406_1408del (p.His469del)	rs775280006
NM_003126.4(SPTA1):c.6421C>T (p.Arg2141Trp)	rs41273519

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