List of variants in gene SLC19A3 reported as likely benign for not provided

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_025243.4(SLC19A3):c.979+105G>A	rs62191374	0.04164
NM_025243.4(SLC19A3):c.-3+142T>G	rs114871078	0.01331
NM_025243.4(SLC19A3):c.1172+227A>G	rs79299809	0.01209
NM_025243.4(SLC19A3):c.*103C>A	rs116590386	0.00909
NM_025243.4(SLC19A3):c.150+233G>A	rs77628307	0.00820
NM_025243.4(SLC19A3):c.1315-64G>A	rs185401751	0.00670
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.-2-3996A>T	rs192316285	0.00510
NM_025243.4(SLC19A3):c.979+292G>A	rs146526874	0.00310
NM_025243.4(SLC19A3):c.1056C>G (p.Phe352Leu)	rs149806390	0.00097
NM_025243.4(SLC19A3):c.801A>G (p.Gln267=)	rs147205930	0.00067
NM_025243.4(SLC19A3):c.987G>A (p.Val329=)	rs146636922	0.00061
NM_025243.4(SLC19A3):c.18T>A (p.Thr6=)	rs141093593	0.00055
NM_025243.4(SLC19A3):c.613A>G (p.Arg205Gly)	rs199558186	0.00041
NM_025243.4(SLC19A3):c.980-46G>T	rs183152800	0.00036
NM_025243.4(SLC19A3):c.387C>T (p.Ser129=)	rs143579160	0.00022
NM_025243.4(SLC19A3):c.99A>G (p.Pro33=)	rs17853011	0.00014
NM_025243.4(SLC19A3):c.325G>A (p.Val109Ile)	rs780569649	0.00009
NM_025243.4(SLC19A3):c.1104T>C (p.Asn368=)	rs767338710	0.00001
NM_025243.4(SLC19A3):c.*8G>A	rs188532608
NM_025243.4(SLC19A3):c.*8G>T	rs188532608
NM_025243.4(SLC19A3):c.123A>T (p.Gly41=)
NM_025243.4(SLC19A3):c.141C>T (p.Thr47=)	rs145710386
NM_025243.4(SLC19A3):c.151-36G>T	rs111818722
NM_025243.4(SLC19A3):c.390G>T (p.Val130=)	rs376187918
NM_025243.4(SLC19A3):c.399C>G (p.Pro133=)	rs138363524
NM_025243.4(SLC19A3):c.555T>C (p.Leu185=)	rs2106329019
NM_025243.4(SLC19A3):c.660T>A (p.Thr220=)	rs777660984
NM_025243.4(SLC19A3):c.980-10T>C	rs750918156

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