List of variants in gene GRHPR reported as not provided for primary hyperoxaluria type 2

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_012203.2(GRHPR):c.579A>G (p.Ala193=)	rs309458	0.85807
NM_012203.2(GRHPR):c.295C>T (p.Arg99Ter)	rs119490108	0.00001
NM_012203.2(GRHPR):c.103del (p.Asp35fs)	rs80356708
NM_012203.2(GRHPR):c.404+3_404+6del	rs180177309

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