Variants in gene SLC3A1 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000341.4(SLC3A1):c.1400T>C (p.Met467Thr)	rs121912691	0.00175
NM_000341.4(SLC3A1):c.592del (p.Ala198fs)	rs778000327	0.00028
NM_000341.4(SLC3A1):c.647C>T (p.Thr216Met)	rs369641941	0.00009
NM_000341.4(SLC3A1):c.1354C>T (p.Arg452Trp)	rs201502095	0.00007
NM_000341.4(SLC3A1):c.1084C>T (p.Arg362Cys)	rs375399468	0.00006
NM_000341.4(SLC3A1):c.1093C>T (p.Arg365Trp)	rs765828196	0.00005
NM_000341.4(SLC3A1):c.1094G>T (p.Arg365Leu)	rs567478582
NM_000341.4(SLC3A1):c.1603_1604del (p.Thr535fs)	rs767801148

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