Variants in gene ABCA12 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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_173076.3(ABCA12):c.2033A>G (p.Asn678Ser)	rs147218173	0.00138
NM_173076.3(ABCA12):c.485C>T (p.Ala162Val)	rs149399707	0.00126
NM_173076.3(ABCA12):c.3481A>T (p.Met1161Leu)	rs141077206	0.00092
NM_173076.3(ABCA12):c.5221C>T (p.Arg1741Cys)	rs141036904	0.00058
NM_173076.3(ABCA12):c.2078C>A (p.Ser693Tyr)	rs148445044	0.00027
NM_173076.3(ABCA12):c.627A>C (p.Lys209Asn)	rs149882663	0.00014

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