List of variants in gene CTLA4 reported as likely pathogenic for thyroid gland disorder

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_005214.5(CTLA4):c.118G>A (p.Val40Met)	rs1553657378
NM_005214.5(CTLA4):c.410C>A (p.Pro137Gln)	rs1553657429
NM_005214.5(CTLA4):c.410C>T (p.Pro137Leu)	rs1553657429

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