List of variants reported as uncertain significance for Chondrocalcinosis by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_054027.6(ANKH):c.*1211del	rs886060082
NM_054027.6(ANKH):c.*1318ATTT[1]	rs886060081
NM_054027.6(ANKH):c.*2113del	rs753413461
NM_054027.6(ANKH):c.*2243C>G	rs531980160
NM_054027.6(ANKH):c.*2301del	rs796083754
NM_054027.6(ANKH):c.*5034del	rs541644826
NM_054027.6(ANKH):c.*5912del	rs765143871
NM_054027.6(ANKH):c.*5912dup	rs765143871
NM_054027.6(ANKH):c.-128_-80delinsCGC	rs886060203
NM_054027.6(ANKH):c.-291CCG[5]	rs531421951
NM_054027.6(ANKH):c.-291CCG[6]	rs531421951
NM_054027.6(ANKH):c.-291CCG[9]	rs531421951
NM_054027.6(ANKH):c.-80_-79insC	rs886060201
NM_054027.6(ANKH):c.-89_-80delinsTC	rs886060202

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