List of variants in gene CAPN1 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_005186.4(CAPN1):c.1781T>C (p.Val594Ala)	rs148743672	0.00236
NM_005186.4(CAPN1):c.1152C>T (p.Cys384=)	rs17881532	0.00229
NM_005186.4(CAPN1):c.1597C>T (p.Pro533Ser)	rs150244086	0.00099
NM_005186.4(CAPN1):c.519G>A (p.Gly173=)	rs201854138	0.00025
NM_005186.4(CAPN1):c.381C>T (p.Asn127=)	rs374553729	0.00005
NM_005186.4(CAPN1):c.189G>C (p.Pro63=)
NM_005186.4(CAPN1):c.621G>T (p.Gly207=)

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