ClinVar Miner

List of variants in gene CHRND, CHRNG studied for Congenital myasthenic syndrome

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_000751.3(CHRND):c.*885T>C	rs1004175	0.34980
NM_000751.3(CHRND):c.*52A>G	rs2767	0.34088
NM_000751.3(CHRND):c.*365C>A	rs112940737	0.00145
NM_000751.3(CHRND):c.*547G>C	rs2343841

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