ClinVar Miner

List of variants in gene ABCB7 reported as likely pathogenic for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_001271696.3(ABCB7):c.1235T>C (p.Met412Thr) rs1057518042

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