Variants in gene ABCA12 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_173076.3(ABCA12):c.4139A>G (p.Asn1380Ser)	rs28940269	0.00005
NM_173076.3(ABCA12):c.4951G>A (p.Gly1651Ser)	rs28940568	0.00003
NM_173076.3(ABCA12):c.179G>C (p.Arg60Pro)	rs762065937
NM_173076.3(ABCA12):c.2273dup (p.Leu758fs)	rs1064794286
NM_173076.3(ABCA12):c.2296C>T (p.Gln766Ter)	rs772046102
NM_173076.3(ABCA12):c.3882G>A (p.Trp1294Ter)	rs1452228678
NM_173076.3(ABCA12):c.5381+1G>C	rs1553523037

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