ClinVar Miner

List of variants reported as likely benign for Griscelli syndrome by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_004580.4(RAB27A):c.*1392A>C rs12907749
NM_004580.4(RAB27A):c.*2067C>G rs7168226
NM_004580.4(RAB27A):c.*2349A>G rs76970799
NM_004580.4(RAB27A):c.*387A>G rs73407873
NM_004580.4(RAB27A):c.*731G>T rs76097718
NM_004580.4(RAB27A):c.*842G>A rs59982153
NM_004580.4(RAB27A):c.-147A>G rs61436564

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.