ClinVar Miner

List of variants in gene SGCG reported by Mayo Clinic Laboratories, Mayo Clinic

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000231.3(SGCG):c.385G>A (p.Gly129Ser)	rs747046381	0.00006
NM_000231.3(SGCG):c.195+5G>A	rs532463691	0.00001
NM_000231.3(SGCG):c.599del (p.Ser200fs)	rs886043860
NM_000231.3(SGCG):c.801_802del (p.Pro268fs)	rs2137534216

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