List of variants in gene SLC19A3 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_025243.4(SLC19A3):c.309G>A (p.Val103=)	rs142837989	0.00618
NM_025243.4(SLC19A3):c.*1995G>A	rs185496445	0.00400
NM_025243.4(SLC19A3):c.*348A>C	rs112957132	0.00364
NM_025243.4(SLC19A3):c.546G>A (p.Val182=)	rs143188189	0.00263
NM_025243.4(SLC19A3):c.*231G>A	rs192321676	0.00153
NM_025243.4(SLC19A3):c.*499C>T	rs182183617	0.00127
NM_025243.4(SLC19A3):c.1132A>G (p.Ile378Val)	rs117864472	0.00062
NM_025243.4(SLC19A3):c.99A>G (p.Pro33=)	rs17853011	0.00014
NM_025243.4(SLC19A3):c.*975G>T	rs371001817	0.00011
NM_025243.4(SLC19A3):c.-60C>T	rs372251558	0.00005
NM_025243.4(SLC19A3):c.*1094C>T	rs111724178
NM_025243.4(SLC19A3):c.*1859C>T	rs78796362
NM_025243.4(SLC19A3):c.*8G>A	rs188532608
NM_025243.4(SLC19A3):c.779A>T (p.Asp260Val)	rs371155923

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