List of variants in gene CSRP3 reported as uncertain significance for Hypertrophic cardiomyopathy

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003476.4(CSRP3):c.-181delC	rs886048102	0.00372
NM_003476.5(CSRP3):c.131T>C (p.Leu44Pro)	rs104894205	0.00006
NM_003476.5(CSRP3):c.230C>G (p.Ala77Gly)	rs772138289	0.00004
NM_003476.5(CSRP3):c.436C>T (p.Arg146Cys)	rs376198883	0.00004
NM_003476.5(CSRP3):c.437G>A (p.Arg146His)	rs377066670	0.00002
NM_003476.5(CSRP3):c.206A>G (p.Lys69Arg)	rs137852764	0.00001
NM_003476.4(CSRP3):c.-161delG	rs138573509
NM_003476.4(CSRP3):c.-162_-161AG[6]	rs886048098
NM_003476.4(CSRP3):c.-180delA	rs34865888
NM_003476.4(CSRP3):c.-182delT	rs886048103
NM_003476.5(CSRP3):c.191G>T (p.Arg64Leu)	rs375014380
NM_003476.5(CSRP3):c.322del (p.Ser108fs)	rs1590103399
NM_003476.5(CSRP3):c.357G>T (p.Lys119Asn)
NM_003476.5(CSRP3):c.511T>G (p.Cys171Gly)	rs770760020

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.