ClinVar Miner

List of variants reported as uncertain significance for chromosome 10 disorder by New York Genome Center

Included ClinVar conditions (8):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_016628.5(WAC):c.1597A>G (p.Asn533Asp)	rs1841460217
NM_016628.5(WAC):c.275-22319G>T	rs2132485043

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