ClinVar Miner

List of variants in gene SRP72 reported as benign for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_006947.4(SRP72):c.*1313C>G rs113719942
NM_006947.4(SRP72):c.*139G>A rs28438730
NM_006947.4(SRP72):c.*1603A>G rs1142851
NM_006947.4(SRP72):c.*173T>C rs10051
NM_006947.4(SRP72):c.*386G>A rs4260596
NM_006947.4(SRP72):c.*442A>G rs7762
NM_006947.4(SRP72):c.*622_*649del rs59791697
NM_006947.4(SRP72):c.*732A>G rs14211
NM_006947.4(SRP72):c.*780C>T rs10518
NM_006947.4(SRP72):c.1410A>G (p.Leu470=) rs17086879
NM_006947.4(SRP72):c.1671A>G (p.Lys557=) rs34419325
NM_006947.4(SRP72):c.19G>T (p.Gly7Trp) rs17524437
NM_006947.4(SRP72):c.21G>T (p.Gly7=) rs12513091
NM_006947.4(SRP72):c.686A>G (p.His229Arg) rs138986942

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