List of variants in gene HOGA1 reported by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 27

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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	0.39537
NM_138413.4(HOGA1):c.835-120A>G	rs1124116	0.34160
NM_138413.4(HOGA1):c.912C>A (p.Ala304=)	rs12261752	0.29673
NM_138413.4(HOGA1):c.*313A>C	rs933057	0.25981
NM_138413.4(HOGA1):c.*560T>C	rs1977641	0.23684
NM_138413.4(HOGA1):c.212-21A>G	rs11817730	0.19877
NM_138413.4(HOGA1):c.700+67G>A	rs2297643	0.16278
NM_138413.4(HOGA1):c.604-85T>C	rs2297644	0.15105
NM_138413.4(HOGA1):c.469-25C>T	rs7078003	0.14259
NM_138413.4(HOGA1):c.469-31C>T	rs75929214	0.09030
NM_138413.4(HOGA1):c.834+230G>A	rs2275050	0.03942
NM_138413.4(HOGA1):c.*360C>T	rs114372258	0.03198
NM_138413.4(HOGA1):c.340+26G>C	rs74155508	0.02786
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.468+191G>A	rs115734824	0.01598
NM_138413.4(HOGA1):c.834+42G>T	rs115279832	0.01504
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.771C>T (p.Cys257=)	rs550989147	0.00015
NM_138413.4(HOGA1):c.*186C>A	rs576078709
NM_138413.4(HOGA1):c.*354dup	rs5787248
NM_138413.4(HOGA1):c.*415T>A	rs148648470
NM_138413.4(HOGA1):c.*637G>A	rs1977640

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