List of variants in gene CHMP2B reported as 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_014043.4(CHMP2B):c.312T>C (p.Thr104=)	rs11540913	0.82371
NM_014043.4(CHMP2B):c.27C>T (p.Thr9=)	rs2279720	0.09131
NM_014043.4(CHMP2B):c.372A>C (p.Thr124=)	rs1044499	0.09006
NM_014043.4(CHMP2B):c.85A>G (p.Ile29Val)	rs63750818	0.00020
NM_014043.4(CHMP2B):c.428A>G (p.Asn143Ser)	rs63750944	0.00004
NM_014043.4(CHMP2B):c.556C>T (p.Arg186Ter)	rs63751048	0.00001
NM_014043.4(CHMP2B):c.94C>T (p.Arg32Ter)	rs763615051	0.00001
NM_014043.4(CHMP2B):c.311C>A (p.Thr104Asn)	rs281864934
NM_014043.4(CHMP2B):c.442G>T (p.Asp148Tyr)	rs63750653
NM_014043.4(CHMP2B):c.493C>T (p.Gln165Ter)	rs63750355
NM_014043.4(CHMP2B):c.532-1G>A	rs63750652
NM_014043.4(CHMP2B):c.532-1G>C	rs63750652
NM_014043.4(CHMP2B):c.618A>C (p.Gln206His)	rs63751126

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