ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance by Clinical Genomics Lab,St. Jude Children's Research Hospital

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_000179.2(MSH6):c.1602C>G (p.Asn534Lys) rs763712971
NM_000179.2(MSH6):c.1657A>C (p.Thr553Pro) rs1294509946
NM_000179.2(MSH6):c.188C>G (p.Ser63Cys) rs587779920
NM_000179.2(MSH6):c.2588A>G (p.Glu863Gly) rs876658238
NM_000179.2(MSH6):c.3961A>G (p.Arg1321Gly) rs41295278
NM_000179.2(MSH6):c.643G>A (p.Val215Ile) rs145959653
NM_000179.2(MSH6):c.749T>C (p.Val250Ala) rs587781275
NM_000179.2(MSH6):c.866_867delinsAA (p.Gly289Glu) rs267608079
NM_000179.2(MSH6):c.905G>C (p.Arg302Thr) rs587781510
NM_000179.2(MSH6):c.942C>G (p.Ser314Arg) rs150440246

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.