ClinVar Miner

List of variants reported as pathogenic for Barrett esophagus by OMIM

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		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_138455.4(CTHRC1):c.131A>C (p.Gln44Pro)	rs387907029	0.00010
NM_138715.3(MSR1):c.760C>G (p.Leu254Val)	rs387906645	0.00003

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