ClinVar Miner

List of variants in gene SGCD reported by Genetics and Genomics Program, Sidra Medicine

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.848A>G (p.Gln283Arg)	rs397516338	0.00019
NM_000337.6(SGCD):c.538A>T (p.Thr180Ser)	rs1187720404

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