ClinVar Miner

List of variants in gene GHRHR reported as pathogenic by Endocrinology Clinic, Seth G.S. Medical College

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: 2

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HGVS	dbSNP	gnomAD frequency
NC_000007.14:g.30959635_30967328delinsAGAGATCCA
NC_000007.14:g.31008681G>T	rs1562606449

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