ClinVar Miner

List of variants in gene SLC39A13 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_001128225.3(SLC39A13):c.1037C>T (p.Pro346Leu) rs35978122 0.00270
NM_001128225.3(SLC39A13):c.571G>A (p.Ala191Thr) rs138998777 0.00061
NM_001128225.3(SLC39A13):c.104C>T (p.Pro35Leu) rs374680665 0.00014
NM_001128225.3(SLC39A13):c.635G>A (p.Arg212Gln) rs200490683 0.00013
NM_001128225.3(SLC39A13):c.1090G>T (p.Val364Leu) rs542593908 0.00006
NM_001128225.3(SLC39A13):c.889G>A (p.Ala297Thr) rs374739509 0.00005
NM_001128225.3(SLC39A13):c.1046C>T (p.Ser349Phe) rs376076637 0.00004
NM_001128225.3(SLC39A13):c.116G>A (p.Ser39Asn) rs775918761 0.00004
NM_001128225.3(SLC39A13):c.640A>G (p.Ile214Val) rs750123189 0.00004
NM_001128225.3(SLC39A13):c.95G>T (p.Gly32Val) rs754558033 0.00004
NM_001128225.3(SLC39A13):c.403A>G (p.Ser135Gly) rs377518253 0.00003
NM_001128225.3(SLC39A13):c.254C>T (p.Pro85Leu) rs763663223 0.00002
NM_001128225.3(SLC39A13):c.584G>A (p.Gly195Asp) rs750069673 0.00002
NM_001128225.3(SLC39A13):c.113G>A (p.Arg38Gln) rs770839268 0.00001
NM_001128225.3(SLC39A13):c.184G>A (p.Gly62Arg) rs200726045 0.00001
NM_001128225.3(SLC39A13):c.284C>T (p.Thr95Ile) rs1317018795 0.00001
NM_001128225.3(SLC39A13):c.313C>T (p.Arg105Cys) rs374468349 0.00001
NM_001128225.3(SLC39A13):c.31A>G (p.Met11Val) rs768592866 0.00001
NM_001128225.3(SLC39A13):c.355G>T (p.Gly119Cys) rs892859231 0.00001
NM_001128225.3(SLC39A13):c.392C>T (p.Ala131Val) rs370161381 0.00001
NM_001128225.3(SLC39A13):c.823G>C (p.Asp275His) rs1484874346 0.00001
NM_001128225.3(SLC39A13):c.-9+3G>T rs920033870
NM_001128225.3(SLC39A13):c.169G>C (p.Gly57Arg) rs2153291239
NM_001128225.3(SLC39A13):c.221G>T (p.Gly74Val) rs121434363
NM_001128225.3(SLC39A13):c.347G>C (p.Gly116Ala)
NM_001128225.3(SLC39A13):c.38G>C (p.Gly13Ala) rs148165667
NM_001128225.3(SLC39A13):c.538-3_541del rs2153298990
NM_001128225.3(SLC39A13):c.542C>A (p.Pro181His) rs776239751
NM_001128225.3(SLC39A13):c.583G>A (p.Gly195Ser) rs1003779948

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