ClinVar Miner

List of variants in gene KRT19 reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002276.5(KRT19):c.471T>C (p.Asn157=) rs4601 0.63838
NM_002276.5(KRT19):c.90C>T (p.Ala30=) rs11550883 0.59102
NM_002276.4(KRT19):c.-99G>C rs56051972 0.29170
NM_002276.5(KRT19):c.552C>T (p.Asn184=) rs267607655 0.00007
NM_002276.5(KRT19):c.49G>A (p.Gly17Ser) rs200777034 0.00001
NM_002276.5(KRT19):c.179C>G (p.Ala60Gly) rs4602
NM_002276.5(KRT19):c.685G>A (p.Val229Met) rs267607654

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.