ClinVar Miner

List of variants reported as benign for beta-thalassemia HBB/LCRB

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NC_000011.10:g.5225416C>T rs113969885
NC_000011.10:g.5227411G>A
NC_000011.10:g.5227540G>A
NM_000518.4(HBB):c.157G>A (p.Asp53Asn) rs33961886
NM_000518.4(HBB):c.410G>A (p.Gly137Asp) rs33949486
NM_000518.4(HBB):c.68A>C (p.Glu23Ala) rs33936254
NM_000518.5(HBB):c.*96T>C rs34029390
NM_000518.5(HBB):c.-31C>T rs63750628
NM_000518.5(HBB):c.-35A>G
NM_000518.5(HBB):c.262A>C (p.Thr88Pro) rs35553496
NM_000518.5(HBB):c.315+16G>C rs10768683
NM_000518.5(HBB):c.315+255T>C
NM_000518.5(HBB):c.315+74T>G rs7480526
NM_000518.5(HBB):c.315+81C>T rs7946748
NM_000518.5(HBB):c.316-185C>T rs1609812
NM_000518.5(HBB):c.316-208C>G
NM_000518.5(HBB):c.316-272G>C rs773343845
NM_000518.5(HBB):c.316-272G>T
NM_000518.5(HBB):c.316-373C>A rs78815705
NM_000518.5(HBB):c.92+13G>T
NM_000518.5(HBB):c.93-23T>C rs111851677
NM_000518.5(HBB):c.9T>C (p.His3=) rs713040

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