ClinVar Miner

List of variants in gene RPS19 reported as likely pathogenic for anemia (disease)

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_001022.3(RPS19):c.356+3A>C rs1555841379
NM_001022.3(RPS19):c.382C>T (p.Gln128Ter) rs1060503688

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