ClinVar Miner

List of variants in gene GARIN4 reported as likely benign for Mobius syndrome

Included ClinVar conditions (1):

Oromandibular-limb hypogenesis spectrum

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
NM_153606.4(GARIN4):c.1465T>C (p.Ser489Pro)	rs767737768	0.00001
NM_153606.4(GARIN4):c.1475G>A (p.Gly492Asp)	rs886037883

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