List of variants in gene QRICH1 reported by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_198880.3(QRICH1):c.1147_1150del (p.Leu383fs)	rs1376687924
NM_198880.3(QRICH1):c.1306C>G (p.Gln436Glu)	rs1575347805
NM_198880.3(QRICH1):c.646G>A (p.Val216Met)	rs76308243
NM_198880.3(QRICH1):c.64dup (p.Val22fs)	rs1575373920

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.