List of variants in gene combination KRIT1, LOC113748416 reported as uncertain significance for cerebral cavernous malformation

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_194454.3(KRIT1):c.-538C>T	rs886062497	0.00048
NM_194456.1(KRIT1):c.-647T>C	rs370781912	0.00034
NM_194456.1(KRIT1):c.-628T>A	rs745344627	0.00025
NM_194454.3(KRIT1):c.-529C>T	rs886062496	0.00006
NM_194456.1(KRIT1):c.-632A>C	rs1800915586

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