Variants in gene MFSD8 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001371596.2(MFSD8):c.1006G>C (p.Glu336Gln)	rs150418024	0.00299
NM_001371596.2(MFSD8):c.590G>A (p.Gly197Asp)	rs28544073	0.00184
NM_001371596.2(MFSD8):c.206C>T (p.Pro69Leu)	rs147750747	0.00013
NM_001371596.2(MFSD8):c.15G>A (p.Arg5=)	rs762559863	0.00001
NM_001371596.2(MFSD8):c.288A>G (p.Leu96=)	rs1008821019	0.00001
NM_001371596.2(MFSD8):c.421T>C (p.Leu141=)	rs778330834	0.00001
NM_001371596.2(MFSD8):c.1470A>G (p.Gly490=)	rs1477527807
NM_001371596.2(MFSD8):c.63-4del	rs755011754

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