List of variants in gene SLC19A3 reported as uncertain significance by GeneDx

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: 41

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HGVS	dbSNP	gnomAD frequency
NM_025243.4(SLC19A3):c.1145G>A (p.Ser382Asn)	rs145288025	0.00073
NM_025243.4(SLC19A3):c.187T>C (p.Tyr63His)	rs144817990	0.00059
NM_025243.4(SLC19A3):c.436G>A (p.Val146Ile)	rs147502239	0.00036
NM_025243.4(SLC19A3):c.1112C>T (p.Ala371Val)	rs142166552	0.00034
NM_025243.4(SLC19A3):c.562C>G (p.Leu188Val)	rs146949876	0.00026
NM_025243.4(SLC19A3):c.1370G>A (p.Ser457Asn)	rs138839321	0.00022
NM_025243.4(SLC19A3):c.106A>G (p.Ile36Val)	rs372637185	0.00019
NM_025243.4(SLC19A3):c.557T>C (p.Phe186Ser)	rs116533505	0.00019
NM_025243.4(SLC19A3):c.977G>T (p.Gly326Val)	rs747823282	0.00016
NM_025243.4(SLC19A3):c.865A>G (p.Thr289Ala)	rs746272588	0.00012
NM_025243.4(SLC19A3):c.1339G>A (p.Ala447Thr)	rs754794859	0.00009
NM_025243.4(SLC19A3):c.373G>A (p.Ala125Thr)	rs996377339	0.00008
NM_025243.4(SLC19A3):c.914A>G (p.Tyr305Cys)	rs189540672	0.00007
NM_025243.4(SLC19A3):c.1343T>C (p.Val448Ala)	rs201544540	0.00006
NM_025243.4(SLC19A3):c.335T>C (p.Phe112Ser)	rs200971390	0.00006
NM_025243.4(SLC19A3):c.980G>A (p.Gly327Glu)	rs1248803297	0.00005
NM_025243.4(SLC19A3):c.1024G>A (p.Asp342Asn)	rs376305641	0.00003
NM_025243.4(SLC19A3):c.500T>A (p.Met167Lys)	rs376414109	0.00003
NM_025243.4(SLC19A3):c.624G>T (p.Lys208Asn)	rs201274864	0.00003
NM_025243.4(SLC19A3):c.217C>T (p.Leu73Phe)	rs373943165	0.00002
NM_025243.4(SLC19A3):c.488C>T (p.Ser163Phe)	rs898880170	0.00002
NM_025243.4(SLC19A3):c.1118A>G (p.Tyr373Cys)	rs1131691470	0.00001
NM_025243.4(SLC19A3):c.1215G>T (p.Leu405Phe)	rs755120020	0.00001
NM_025243.4(SLC19A3):c.1463G>C (p.Ser488Thr)	rs540774490	0.00001
NM_025243.4(SLC19A3):c.151A>G (p.Ile51Val)	rs764398318	0.00001
NM_025243.4(SLC19A3):c.355G>A (p.Ala119Thr)	rs367620430	0.00001
NM_025243.4(SLC19A3):c.461G>A (p.Gly154Glu)	rs202145913	0.00001
NM_025243.4(SLC19A3):c.611G>A (p.Ser204Asn)	rs773705000	0.00001
NM_025243.4(SLC19A3):c.697C>G (p.Pro233Ala)	rs756864477	0.00001
NM_025243.4(SLC19A3):c.955G>A (p.Val319Ile)	rs372511010	0.00001
NM_025243.4(SLC19A3):c.113A>G (p.Tyr38Cys)	rs766975844
NM_025243.4(SLC19A3):c.1148A>G (p.Tyr383Cys)	rs1057524556
NM_025243.4(SLC19A3):c.1204C>G (p.Arg402Gly)	rs150523975
NM_025243.4(SLC19A3):c.1204C>T (p.Arg402Cys)	rs150523975
NM_025243.4(SLC19A3):c.355G>T (p.Ala119Ser)	rs367620430
NM_025243.4(SLC19A3):c.39T>G (p.Ile13Met)	rs2106332726
NM_025243.4(SLC19A3):c.472G>A (p.Ala158Thr)	rs2106329144
NM_025243.4(SLC19A3):c.488C>A (p.Ser163Tyr)	rs898880170
NM_025243.4(SLC19A3):c.58T>A (p.Cys20Ser)
NM_025243.4(SLC19A3):c.718A>C (p.Thr240Pro)
NM_025243.4(SLC19A3):c.862G>C (p.Ala288Pro)	rs542566978

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