ClinVar Miner

List of variants in gene SLC46A1 reported as uncertain significance for anemia (disease)

Included ClinVar conditions (263):
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Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_080669.6(SLC46A1):c.-67G>T rs782796764
NM_080669.6(SLC46A1):c.158C>T (p.Ala53Val) rs41297069
NM_080669.6(SLC46A1):c.22C>T (p.Pro8Ser) rs41297065
NM_080669.6(SLC46A1):c.294C>A (p.Leu98=) rs371270310
NM_080669.6(SLC46A1):c.462C>T (p.Leu154=) rs782480845
NM_080669.6(SLC46A1):c.512T>A (p.Val171Asp) rs189103810
NM_080669.6(SLC46A1):c.623A>T (p.Tyr208Phe) rs201837257
NM_080669.6(SLC46A1):c.642G>A (p.Leu214=) rs145398587
NM_080669.6(SLC46A1):c.667A>T (p.Thr223Ser) rs886052756
NM_080669.6(SLC46A1):c.752T>C (p.Ile251Thr) rs782457383
NM_080669.6(SLC46A1):c.904A>C (p.Lys302Gln) rs886052755

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