List of variants in gene combination LOC128706665, LOC128706666, MKKS reported as uncertain significance for MKKS-related ciliopathy

Minimum submission review status:		Collection method:
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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_170784.3(MKKS):c.-384C>T	rs568811798	0.00099
NM_170784.3(MKKS):c.-495C>A	rs536112369	0.00064
NM_170784.3(MKKS):c.-496T>G	rs554863155	0.00064
NM_170784.3(MKKS):c.-557A>G	rs145467994	0.00041
NM_170784.3(MKKS):c.-306A>G	rs3748466	0.00028
NM_170784.3(MKKS):c.-477G>T	rs886056501	0.00009
NM_170784.3(MKKS):c.-388A>G	rs945662294	0.00001
NM_170784.3(MKKS):c.-481T>A	rs886056502	0.00001
NM_170784.3(MKKS):c.-562C>T	rs886056503	0.00001
NM_170784.3(MKKS):c.-649+2366C>T	rs886056504	0.00001
NM_170784.3(MKKS):c.-406G>C	rs886056500
NM_170784.3(MKKS):c.-417-13dup	rs528193828
NM_170784.3(MKKS):c.-649+2238A>T	rs541967798
NM_170784.3(MKKS):c.-649+2292del	rs566962031

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