ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as benign for not specified

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Total variants: 6
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HGVS dbSNP
NM_000518.4(HBB):c.130G>C (p.Glu44Gln) rs33922842
NM_000518.4(HBB):c.157G>A (p.Asp53Asn) rs33961886
NM_000518.4(HBB):c.263C>T (p.Thr88Ile) rs33993568
NM_000518.5(HBB):c.170G>A (p.Gly57Asp) rs34439278
NM_000518.5(HBB):c.93-23T>C rs111851677
NM_000518.5(HBB):c.9T>C (p.His3=) rs713040

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