ClinVar Miner

List of variants reported as uncertain significance for Barrett esophagus

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001198800.3(ASCC1):c.778C>T (p.Arg260Cys)
NM_138715.3(MSR1):c.217G>A (p.Ala73Thr)
NM_138715.3(MSR1):c.877C>T (p.Arg293Ter)	rs41341748

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