List of variants in gene RAB18 reported as uncertain significance for Warburg micro syndrome

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_021252.5(RAB18):c.*150C>T	rs768390542
NM_021252.5(RAB18):c.*16A>G	rs886046968
NM_021252.5(RAB18):c.*2030G>T	rs750141100
NM_021252.5(RAB18):c.3046_3047dup	rs886046976
NM_021252.5(RAB18):c.*3293del	rs573606717
NM_021252.5(RAB18):c.*3599dup	rs779470678
NM_021252.5(RAB18):c.*3701GACT[1]	rs759695566

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