List of variants in gene GRHPR reported as uncertain significance by Clinical Biochemistry Laboratory, Health Services Laboratory

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: 14

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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.579= (p.Ala193=)	rs309458	0.14193
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.493+27C>T	rs146896070	0.00432
NM_012203.2(GRHPR):c.598+145G>T	rs72739643	0.00108
NM_012203.1(GRHPR):c.866-25CT[9]	rs34302950
NM_012203.2(GRHPR):c.211G>A (p.Ala71Thr)
NM_012203.2(GRHPR):c.215-11C>T	rs796052076
NM_012203.2(GRHPR):c.638T>C (p.Val213Ala)
NM_012203.2(GRHPR):c.83+52del	rs35891798
NM_012203.2(GRHPR):c.961C>G (p.Pro321Ala)

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