ClinVar Miner

List of variants in gene SATB2 reported by Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001172509.2(SATB2):c.1166G>C (p.Arg389Pro)
NM_001172509.2(SATB2):c.1174G>C (p.Gly392Arg)	rs1688108689
NM_001172509.2(SATB2):c.1610del (p.Asn537fs)	rs1574492395
NM_001172509.2(SATB2):c.597+1G>A	rs1559016679

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