ClinVar Miner

List of variants in gene STX11 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003764.4(STX11):c.616G>A (p.Glu206Lys)	rs145347140	0.00086
NM_003764.4(STX11):c.100G>A (p.Val34Met)	rs777686678
NM_003764.4(STX11):c.764A>C (p.Tyr255Ser)	rs758653019

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