List of variants in gene ABCC6 reported as likely benign for not specified

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001171.6(ABCC6):c.662+12C>T	rs1555520951	0.01842
NM_001171.6(ABCC6):c.2836C>A (p.Leu946Ile)	rs61340537	0.01730
NM_001171.6(ABCC6):c.474+13G>A	rs111339199	0.01326
NM_001171.6(ABCC6):c.1815C>T (p.Leu605=)	rs61318127	0.00732
NM_001171.6(ABCC6):c.1263C>T (p.Thr421=)	rs114179357	0.00180
NM_001171.6(ABCC6):c.396A>G (p.Ser132=)	rs913912489	0.00025
NM_001171.6(ABCC6):c.3735+18G>A	rs562368920	0.00008
NM_001171.6(ABCC6):c.2820T>G (p.Arg940=)	rs72664286	0.00003
NM_001171.6(ABCC6):c.1077A>C (p.Ser359=)	rs72664283
NM_001171.6(ABCC6):c.336C>A (p.Leu112=)	rs971059840
NM_001171.6(ABCC6):c.754C>T (p.Leu252Phe)	rs72653757

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.