List of variants in gene CHCHD10 reported as benign for amyotrophic lateral sclerosis

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_213720.3(CHCHD10):c.261+11A>G	rs131444	0.92009
NM_213720.3(CHCHD10):c.48A>C (p.Pro16=)	rs179468	0.91291
NM_213720.3(CHCHD10):c.286C>A (p.Pro96Thr)	rs111677724	0.05376
NM_213720.3(CHCHD10):c.42-7C>G	rs567239313	0.01558
NM_213720.3(CHCHD10):c.234G>A (p.Ser78=)	rs111527940	0.00755
NM_213720.3(CHCHD10):c.136G>T (p.Ala46Ser)	rs200831077	0.00420
NM_213720.3(CHCHD10):c.330G>A (p.Leu110=)	rs138183274	0.00227
NM_213720.3(CHCHD10):c.41+7G>A	rs141526972	0.00147
NM_213720.3(CHCHD10):c.312C>T (p.Tyr104=)	rs9153
NM_213720.3(CHCHD10):c.409+27G>C	rs140182

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