List of variants in gene CHRND reported as likely benign by PreventionGenetics, part of Exact Sciences

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_000751.3(CHRND):c.1372-50T>G	rs115577037	0.00717
NM_000751.3(CHRND):c.862C>G (p.Gln288Glu)	rs41265127	0.00239
NM_000751.3(CHRND):c.1400G>A (p.Arg467His)	rs148939701	0.00096
NM_000751.3(CHRND):c.817G>A (p.Asp273Asn)	rs202209156	0.00051
NM_000751.3(CHRND):c.408C>T (p.Tyr136=)	rs112921420	0.00046
NM_000751.3(CHRND):c.198+14C>T	rs199538903	0.00036
NM_000751.3(CHRND):c.619+4C>A	rs367936158	0.00032
NM_000751.3(CHRND):c.620-7C>T	rs532055784	0.00011
NM_000751.3(CHRND):c.411C>T (p.Gly137=)	rs373578965	0.00008
NM_000751.3(CHRND):c.620-8G>A	rs377074477	0.00007
NM_000751.3(CHRND):c.646C>T (p.Arg216Trp)	rs777271963	0.00003
NM_000751.3(CHRND):c.52+7G>A	rs1388167579	0.00001
NM_000751.3(CHRND):c.821-52_821-18del	rs530117757

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