ClinVar Miner

List of variants in gene NKX3-2 reported as likely benign for Connective tissue 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001189.4(NKX3-2):c.235A>T (p.Thr79Ser)	rs200167000	0.00283
NM_001189.4(NKX3-2):c.190G>C (p.Gly64Arg)	rs202195290

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