ClinVar Miner

List of variants in gene CLDN19 reported by Neuberg Centre For Genomic Medicine, NCGM

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_148960.3(CLDN19):c.59G>A (p.Gly20Asp)	rs118203979	0.00003
NM_148960.3(CLDN19):c.473+1G>T	rs2524364170
NM_148960.3(CLDN19):c.535G>C (p.Gly179Arg)	rs145591298

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