List of variants in gene GCM2 studied for Hyperparathyroidism 4

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_004752.4(GCM2):c.1181A>C (p.Tyr394Ser)	rs142287570	0.00050
NM_004752.3(GCM2):c.[1136T>A;751C>G]
NM_004752.4(GCM2):c.1003C>T (p.Pro335Ser)
NM_004752.4(GCM2):c.1166T>C (p.Val389Ala)
NM_004752.4(GCM2):c.1398G>C (p.Glu466Asp)	rs537546612
NM_004752.4(GCM2):c.139C>T (p.Arg47Cys)
NM_004752.4(GCM2):c.1A>G (p.Met1Val)	rs2113257238
NM_004752.4(GCM2):c.523A>T (p.Ile175Phe)

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