List of variants in gene COLGALT1 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_024656.4(COLGALT1):c.888C>T (p.Arg296=)	rs146222720	0.00007
NM_024656.4(COLGALT1):c.303G>C (p.Leu101=)	rs372571154	0.00005
NM_024656.4(COLGALT1):c.1275C>T (p.Asp425=)
NM_024656.4(COLGALT1):c.168C>T (p.Ile56=)
NM_024656.4(COLGALT1):c.648C>T (p.Ala216=)	rs2076292951
NM_024656.4(COLGALT1):c.677G>A (p.Arg226Gln)
NM_024656.4(COLGALT1):c.915C>T (p.Ala305=)

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