List of variants in gene RAB18 reported as benign for Warburg micro syndrome 3

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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: 29

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HGVS	dbSNP	gnomAD frequency
NM_021252.5(RAB18):c.*3453G>A	rs11015861	0.43562
NM_021252.5(RAB18):c.*3696T>A	rs10829269	0.19806
NM_021252.5(RAB18):c.*3484T>C	rs11598268	0.17485
NM_021252.5(RAB18):c.*3476A>G	rs11597728	0.17476
NM_021252.5(RAB18):c.*2375A>G	rs2477317	0.06862
NM_021252.5(RAB18):c.*2744C>T	rs12254670	0.03950
NM_021252.5(RAB18):c.*2449A>G	rs12260532	0.03947
NM_021252.5(RAB18):c.*1412C>T	rs10508723	0.03943
NM_021252.5(RAB18):c.*2476G>A	rs12267298	0.03943
NM_021252.5(RAB18):c.*387C>A	rs12248740	0.03936
NM_021252.5(RAB18):c.592G>A (p.Ala198Thr)	rs11015859	0.02882
NM_021252.5(RAB18):c.*3584C>T	rs11015862	0.02826
NM_021252.5(RAB18):c.*3129C>T	rs78270485	0.02396
NM_021252.5(RAB18):c.*757G>T	rs76051289	0.02074
NM_021252.5(RAB18):c.*3939A>T	rs1047915	0.01932
NM_021252.5(RAB18):c.260-7dup	rs142609338	0.01674
NM_021252.5(RAB18):c.*1542T>C	rs10508724	0.01545
NM_021252.5(RAB18):c.*504A>G	rs12571836	0.01543
NM_021252.5(RAB18):c.*278A>T	rs41282848	0.00905
NM_021252.5(RAB18):c.*758A>T	rs10508722	0.00879
NM_021252.4(RAB18):c.-83C>A	rs115326586	0.00616
NM_021252.5(RAB18):c.*1488A>C	rs148630305	0.00510
NM_021252.5(RAB18):c.-20C>T	rs74127323	0.00438
NM_021252.5(RAB18):c.*2529G>A	rs145293804	0.00250
NM_021252.5(RAB18):c.*4131A>G	rs540759797	0.00212
NM_021252.5(RAB18):c.*3521C>T	rs142174174	0.00208
NM_021252.5(RAB18):c.*3967T>C	rs571495776	0.00145
NM_021252.5(RAB18):c.*448G>A	rs563981728	0.00006
NM_021252.5(RAB18):c.260-43_260-42del	rs72201756

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