ClinVar Miner

List of variants in gene ASCC1 studied for Barrett esophagus

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001198800.3(ASCC1):c.869A>G (p.Asn290Ser)	rs146370051	0.00135
NM_001198800.3(ASCC1):c.714C>A (p.Tyr238Ter)	rs138245920
NM_001198800.3(ASCC1):c.778C>T (p.Arg260Cys)

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