List of variants in gene HOGA1 reported as benign for primary hyperoxaluria

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_138413.4(HOGA1):c.*445A>G	rs1812286	0.40584
NM_138413.4(HOGA1):c.*498G>A	rs2018017	0.40451
NM_138413.4(HOGA1):c.*355C>T	rs1977642	0.40312
NM_138413.4(HOGA1):c.835-120A>G	rs1124116	0.34185
NM_138413.4(HOGA1):c.912C>A (p.Ala304=)	rs12261752	0.29673
NM_138413.4(HOGA1):c.*313A>C	rs933057	0.26438
NM_138413.4(HOGA1):c.396G>A (p.Ala132=)	rs41290456	0.02716
NM_138413.4(HOGA1):c.-279G>A	rs41309988	0.02511
NM_138413.4(HOGA1):c.777G>A (p.Thr259=)	rs34820265	0.01024
NM_138413.4(HOGA1):c.*94C>T	rs116711005	0.00688
NM_138413.4(HOGA1):c.700+7C>T	rs57616820	0.00367
NM_138413.4(HOGA1):c.284G>A (p.Arg95His)	rs754634699	0.00009
NM_138413.4(HOGA1):c.*560T>C	rs1977641
NM_138413.4(HOGA1):c.*637G>A	rs1977640

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