List of variants in gene KRIT1 reported as benign for not provided

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_194454.3(KRIT1):c.989+63C>G	rs2027950	0.57036
NM_194454.3(KRIT1):c.1818+146A>G	rs74603220	0.10873
NM_194454.3(KRIT1):c.1980A>G (p.Val660=)	rs11542682	0.10861
NM_194454.3(KRIT1):c.729+240G>T	rs73407588	0.03646
NM_194454.3(KRIT1):c.*272G>A	rs28502064	0.02669
NM_194454.3(KRIT1):c.486-193T>C	rs75654928	0.01703
NM_194454.3(KRIT1):c.*141C>T	rs117325194	0.00554
NM_194454.3(KRIT1):c.1095A>G (p.Gly365=)	rs143710815	0.00238
NM_194454.3(KRIT1):c.*132T>G	rs572414111	0.00138
NM_194454.3(KRIT1):c.*137del	rs543954194	0.00138
NM_194454.3(KRIT1):c.1255-296del	rs568078150
NM_194454.3(KRIT1):c.1411+181G>A	rs112410984
NM_194454.3(KRIT1):c.1564-316A>T	rs10271533
NM_194454.3(KRIT1):c.485+65G>C	rs17164451
NM_194454.3(KRIT1):c.730-93A>G	rs73407587

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