List of variants in gene GJA5 reported as uncertain significance for chromosomal disorder

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_181703.4(GJA5):c.995G>A (p.Arg332His)	rs116551187	0.00037
NM_181703.4(GJA5):c.365C>T (p.Ser122Phe)	rs781831348	0.00006

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