Variants in gene SLC19A3 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_025243.4(SLC19A3):c.1049T>C (p.Val350Ala)	rs34507036	0.09001
NM_025243.4(SLC19A3):c.435C>T (p.Ser145=)	rs76517176	0.04500
NM_025243.4(SLC19A3):c.549T>C (p.Ala183=)	rs74693100	0.04490
NM_025243.4(SLC19A3):c.520G>A (p.Val174Ile)	rs59736804	0.03276
NM_025243.4(SLC19A3):c.42C>T (p.Tyr14=)	rs34080459	0.01664
NM_025243.4(SLC19A3):c.309G>A (p.Val103=)	rs142837989	0.00618
NM_025243.4(SLC19A3):c.421G>A (p.Gly141Ser)	rs148144444	0.00577
NM_025243.4(SLC19A3):c.546G>A (p.Val182=)	rs143188189	0.00263
NM_025243.4(SLC19A3):c.621A>G (p.Ile207Met)	rs145804755	0.00150
NM_025243.4(SLC19A3):c.1132A>G (p.Ile378Val)	rs117864472	0.00062
NM_025243.4(SLC19A3):c.18T>A (p.Thr6=)	rs141093593	0.00055
NM_025243.4(SLC19A3):c.99A>G (p.Pro33=)	rs17853011	0.00014
NM_025243.4(SLC19A3):c.1252C>G (p.Gln418Glu)	rs368364131	0.00001
NM_025243.4(SLC19A3):c.*8G>A	rs188532608
NM_025243.4(SLC19A3):c.390G>T (p.Val130=)	rs376187918

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