List of variants in gene ADAM9 reported as likely 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: 4

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 8p11.22(chr8:38933032-38935086)x1
NM_003816.3(ADAM9):c.1881+1G>A	rs1838882266
NM_003816.3(ADAM9):c.254+1G>A
NM_003816.3(ADAM9):c.744+1G>A

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