ClinVar Miner

List of variants in gene SLC25A38 reported as benign for anemia (disease)

Included ClinVar conditions (264):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_017875.4(SLC25A38):c.*310A>T rs12991
NM_017875.4(SLC25A38):c.*642del rs34288981
NM_017875.4(SLC25A38):c.165G>A (p.Leu55=) rs2270770

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