List of variants in gene HTRA2 reported as uncertain significance by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_013247.5(HTRA2):c.1010G>A (p.Arg337His)	rs147035021	0.00005
NM_013247.5(HTRA2):c.18G>A (p.Ala6=)	rs372441631	0.00003
NM_013247.5(HTRA2):c.434G>A (p.Ser145Asn)	rs369700396	0.00002
NM_013247.5(HTRA2):c.62G>C (p.Gly21Ala)	rs768870295	0.00001
NM_013247.5(HTRA2):c.1096A>C (p.Met366Leu)	rs747906888
NM_013247.5(HTRA2):c.301A>G (p.Thr101Ala)	rs1675491370
NM_013247.5(HTRA2):c.400G>A (p.Ala134Thr)
NM_013247.5(HTRA2):c.463_465del (p.Glu155del)	rs1021071226
NM_013247.5(HTRA2):c.529G>A (p.Val177Ile)
NM_013247.5(HTRA2):c.618C>A (p.Val206=)	rs186272815
NM_013247.5(HTRA2):c.67A>G (p.Ile23Val)
NM_013247.5(HTRA2):c.8C>T (p.Ala3Val)
NM_013247.5(HTRA2):c.968T>G (p.Met323Arg)	rs1553395110

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