List of variants in gene GALNT3 reported as likely benign for endocrine gland neoplasm

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004482.4(GALNT3):c.901G>A (p.Val301Ile)	rs143647583	0.00222
NM_004482.4(GALNT3):c.189G>A (p.Leu63=)	rs188814778	0.00041
NM_004482.4(GALNT3):c.504T>C (p.Thr168=)	rs183709224	0.00015
NM_004482.4(GALNT3):c.1194A>G (p.Val398=)	rs150937941	0.00011
NM_004482.4(GALNT3):c.897G>T (p.Thr299=)	rs75931918

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