List of variants in gene CHRND reported as benign by Invitae

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_000751.3(CHRND):c.12A>G (p.Pro4=)	rs2245601	0.45730
NM_000751.3(CHRND):c.1047+9T>C	rs3762528	0.07349
NM_000751.3(CHRND):c.120G>A (p.Lys40=)	rs55921262	0.03225
NM_000751.3(CHRND):c.243C>T (p.His81=)	rs115841867	0.00919
NM_000751.3(CHRND):c.932+20G>A	rs114022008	0.00793
NM_000751.3(CHRND):c.1253-8G>A	rs144545619	0.00548
NM_000751.3(CHRND):c.1371+7G>T	rs188395796	0.00350
NM_000751.3(CHRND):c.1105C>T (p.Pro369Ser)	rs2229194	0.00305
NM_000751.3(CHRND):c.117C>G (p.Asn39Lys)	rs77084550	0.00300
NM_000751.3(CHRND):c.414C>T (p.Phe138=)	rs150208750	0.00265
NM_000751.3(CHRND):c.862C>G (p.Gln288Glu)	rs41265127	0.00239
NM_000751.3(CHRND):c.1530C>T (p.Asn510=)	rs114463490	0.00175
NM_000751.3(CHRND):c.1253-9C>T	rs2853458	0.00057
NM_000751.3(CHRND):c.199-19C>T	rs145984749	0.00013
NM_000751.3(CHRND):c.525G>A (p.Thr175=)	rs56203086	0.00009
NM_000751.3(CHRND):c.620-8G>A	rs377074477	0.00007
NM_000751.3(CHRND):c.1477G>A (p.Val493Ile)	rs567130034	0.00006
NM_000751.3(CHRND):c.1252+10C>T	rs373581541	0.00004
NM_000751.3(CHRND):c.611G>T (p.Gly204Val)	rs531000772	0.00004
NM_000751.3(CHRND):c.267G>C (p.Lys89Asn)	rs545298641

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