List of variants in gene KRIT1 reported as likely benign by GeneDx

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_194454.3(KRIT1):c.1095A>G (p.Gly365=)	rs143710815	0.00238
NM_194454.3(KRIT1):c.1140G>A (p.Thr380=)	rs140009885	0.00187
NM_194454.3(KRIT1):c.1819-12G>C	rs199748245	0.00097
NM_194454.3(KRIT1):c.1412-9G>A	rs199932606	0.00043
NM_194454.3(KRIT1):c.2136A>G (p.Thr712=)	rs745397726	0.00001
NM_194454.3(KRIT1):c.1563+10G>A	rs1554512600

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