List of variants in gene ELOC reported as likely pathogenic for papillary adenocarcinoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
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_005648.4(ELOC):c.235T>A (p.Tyr79Asn)	rs1057519974
NM_005648.4(ELOC):c.236A>C (p.Tyr79Ser)	rs1057519973
NM_005648.4(ELOC):c.236A>T (p.Tyr79Phe)	rs1057519973

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