Variants in gene GRHPR with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_012203.2(GRHPR):c.288-11C>T	rs2736664	0.92549
NM_012203.2(GRHPR):c.494-68A>G	rs309459	0.86126
NM_012203.2(GRHPR):c.579A>G (p.Ala193=)	rs309458	0.85807
NM_012203.2(GRHPR):c.734+9G>A	rs56401536	0.04769
NM_012203.2(GRHPR):c.963G>A (p.Pro321=)	rs76299266	0.01042
NM_012203.2(GRHPR):c.801A>C (p.Gly267=)	rs141800325	0.00078
NM_012203.1(GRHPR):c.866-25CT[9]	rs34302950
NM_012203.2(GRHPR):c.83+52del	rs35891798

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