ClinVar Miner

List of variants in gene GAN reported as pathogenic for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_022041.4(GAN):c.851+1G>A	rs747291494	0.00001
GRCh37/hg19 16q23.2(chr16:81380493-81433070)x1
NM_022041.4(GAN):c.633+2T>C	rs879254001

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