ClinVar Miner

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

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_001022.3(RPS19):c.*54T>C rs527896025
NM_001022.3(RPS19):c.-234G>A rs142324259
NM_001022.3(RPS19):c.-274T>C rs77406992
NM_001022.3(RPS19):c.-288A>C rs192556926
NM_001022.3(RPS19):c.1-14A>G rs201317022
NM_001022.3(RPS19):c.411+12G>A rs61762296
NM_001022.3(RPS19):c.60C>G (p.Ala20=) rs149249194
NM_001022.3(RPS19):c.68A>G (p.Lys23Arg) rs143477104
NM_001022.3(RPS19):c.72-10T>G rs1176399879
NM_001022.3(RPS19):c.72-92A>G rs566047445
NM_001022.3(RPS19):c.75C>T (p.Ser25=) rs370343297

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