Variants in gene GRHPR with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_012203.2(GRHPR):c.734+9G>A	rs56401536	0.04451
NM_012203.2(GRHPR):c.509G>A (p.Arg170Gln)	rs12002324	0.01126
NM_012203.2(GRHPR):c.963G>A (p.Pro321=)	rs76299266	0.01042
NM_012203.2(GRHPR):c.493+9C>T	rs41303225	0.00873
NM_012203.2(GRHPR):c.962C>T (p.Pro321Leu)	rs142356700	0.00442
NM_012203.2(GRHPR):c.512G>A (p.Arg171His)	rs200106110	0.00151
NM_012203.2(GRHPR):c.16C>T (p.Leu6Phe)	rs147185003	0.00129
NM_012203.2(GRHPR):c.234C>T (p.Ile78=)	rs143337459	0.00080
NM_012203.2(GRHPR):c.801A>C (p.Gly267=)	rs141800325	0.00077
NM_012203.2(GRHPR):c.357A>G (p.Leu119=)	rs186922220	0.00008

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