List of variants in gene CHM reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000390.4(CHM):c.29A>G (p.Asp10Gly)	rs138374611	0.00041
NM_000390.4(CHM):c.162A>G (p.Gly54=)	rs138972750	0.00030
NM_000390.4(CHM):c.1758T>C (p.Asn586=)	rs757386474	0.00005
NM_000390.4(CHM):c.1008T>C (p.Ile336=)	rs749991144	0.00003
NM_000390.4(CHM):c.1272T>C (p.Gly424=)	rs764033800	0.00001
NM_000390.4(CHM):c.1737T>C (p.Asp579=)	rs756159060	0.00001
NM_000390.4(CHM):c.1377A>T (p.Thr459=)	rs1171424639

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