List of variants in gene HOGA1 reported as uncertain significance by Natera, Inc.

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_138413.4(HOGA1):c.931C>T (p.Pro311Ser)	rs116455504	0.00047
NM_138413.4(HOGA1):c.299T>C (p.Met100Thr)	rs201630144	0.00021
NM_138413.4(HOGA1):c.554C>T (p.Thr185Met)	rs115282699	0.00019
NM_138413.4(HOGA1):c.106G>A (p.Ala36Thr)	rs573292460	0.00017
NM_138413.4(HOGA1):c.771C>T (p.Cys257=)	rs550989147	0.00015
NM_138413.4(HOGA1):c.701-7C>T	rs372897096	0.00005
NM_138413.4(HOGA1):c.764G>A (p.Arg255Gln)	rs201145417	0.00005
NM_138413.4(HOGA1):c.216C>T (p.Phe72=)	rs780606715	0.00004
NM_138413.4(HOGA1):c.443C>T (p.Ala148Val)	rs149896778	0.00004
NM_138413.4(HOGA1):c.720C>T (p.Cys240=)	rs183301169	0.00004
NM_138413.4(HOGA1):c.407T>C (p.Val136Ala)	rs776292240	0.00003
NM_138413.4(HOGA1):c.133C>G (p.Pro45Ala)	rs1380918472	0.00001
NM_138413.4(HOGA1):c.238G>A (p.Glu80Lys)	rs772441887	0.00001
NM_138413.4(HOGA1):c.260G>C (p.Ser87Thr)	rs1167209340	0.00001
NM_138413.4(HOGA1):c.294G>A (p.Gln98=)	rs777208958	0.00001
NM_138413.4(HOGA1):c.317T>A (p.Leu106Gln)	rs892512382	0.00001
NM_138413.4(HOGA1):c.33G>T (p.Arg11Ser)	rs778696295	0.00001
NM_138413.4(HOGA1):c.420C>T (p.Tyr140=)	rs749899995	0.00001
NM_138413.4(HOGA1):c.832G>A (p.Ala278Thr)	rs748335042	0.00001
NM_138413.4(HOGA1):c.139A>C (p.Thr47Pro)	rs1221444661
NM_138413.4(HOGA1):c.18C>T (p.Val6=)	rs1589899135
NM_138413.4(HOGA1):c.341-8T>C	rs2041094866
NM_138413.4(HOGA1):c.344C>G (p.Thr115Ser)	rs2041094955
NM_138413.4(HOGA1):c.477T>C (p.Asp159=)	rs2041100859
NM_138413.4(HOGA1):c.64G>A (p.Val22Met)	rs1425518232
NM_138413.4(HOGA1):c.835-7T>A	rs768061627

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