ClinVar Miner

List of variants in gene RPS7 studied for anemia (disease)

Included ClinVar conditions (262):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_001011.4(RPS7):c.*31C>T rs191506876
NM_001011.4(RPS7):c.-104G>A rs371620447
NM_001011.4(RPS7):c.-109C>T rs142444366
NM_001011.4(RPS7):c.-13C>T rs765604580
NM_001011.4(RPS7):c.-19+13C>T rs530845583
NM_001011.4(RPS7):c.-23G>A rs886055985
NM_001011.4(RPS7):c.-27C>T rs573443780
NM_001011.4(RPS7):c.-36A>C rs17552296
NM_001011.4(RPS7):c.-44C>T rs563293592
NM_001011.4(RPS7):c.-47G>T rs11558965
NM_001011.4(RPS7):c.-86C>T rs186304514
NM_001011.4(RPS7):c.147+1G>A rs397507554
NM_001011.4(RPS7):c.273T>C (p.His91=) rs1442216854
NM_001011.4(RPS7):c.274_276GTC[1] (p.Val93del) rs1553342919
NM_001011.4(RPS7):c.292-9A>T rs746941533
NM_001011.4(RPS7):c.357-3dup rs140914434
NM_001011.4(RPS7):c.39C>T (p.Gly13=) rs746686516
NM_001011.4(RPS7):c.433C>T (p.Arg145Cys)
NM_001011.4(RPS7):c.435C>T (p.Arg145=) rs142207795
NM_001011.4(RPS7):c.508-12C>A rs2071639
NM_001011.4(RPS7):c.518T>C (p.Phe173Ser) rs1558474062
NM_001011.4(RPS7):c.519T>A (p.Phe173Leu)
NM_001011.4(RPS7):c.75+13C>T rs751796318
NM_001011.4(RPS7):c.76-1G>T rs1057519624

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