List of variants in gene UBIAD1 reported as benign by Illumina Laboratory Services, Illumina

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_013319.3(UBIAD1):c.*904T>C	rs3765906	0.16890
NM_013319.3(UBIAD1):c.*1304C>T	rs17036631	0.09921
NM_013319.3(UBIAD1):c.*1532C>T	rs77270119	0.07082
NM_013319.3(UBIAD1):c.-47T>G	rs72856992	0.05898
NM_013319.3(UBIAD1):c.*148A>G	rs11580061	0.02447
NM_013319.3(UBIAD1):c.*1060G>A	rs115210853	0.01873
NM_013319.3(UBIAD1):c.*819G>A	rs75287995	0.01442
NM_013319.3(UBIAD1):c.-195G>A	rs114907127	0.00966
NM_013319.3(UBIAD1):c.224C>T (p.Ser75Phe)	rs114000606	0.00811
NM_013319.3(UBIAD1):c.*1564C>T	rs111893018	0.00446
NM_013319.3(UBIAD1):c.*552G>A	rs111991610	0.00446
NM_013319.3(UBIAD1):c.*420C>T	rs112789142	0.00444
NM_013319.3(UBIAD1):c.867C>T (p.Thr289=)	rs113307594	0.00340
NM_013319.3(UBIAD1):c.*467G>A	rs112285480	0.00235
NM_013319.3(UBIAD1):c.452A>G (p.Tyr151Cys)	rs138443305	0.00176
NM_013319.3(UBIAD1):c.*18C>T	rs191663672	0.00162
NM_013319.3(UBIAD1):c.*684C>A	rs375520410	0.00151
NM_013319.3(UBIAD1):c.298T>G (p.Leu100Val)	rs140612649	0.00036
NM_013319.3(UBIAD1):c.837C>T (p.Cys279=)	rs201111281	0.00035
NM_013319.3(UBIAD1):c.*1671G>A	rs544393884	0.00014
NM_013319.3(UBIAD1):c.370C>A (p.Arg124=)	rs748615089	0.00004
NM_013319.3(UBIAD1):c.417C>T (p.Tyr139=)	rs377764711	0.00004
NM_013319.3(UBIAD1):c.1817_1820del	rs371474267
NM_013319.3(UBIAD1):c.*48A>G	rs368504935
NM_013319.3(UBIAD1):c.969_970insTTTG	rs3063961

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