ClinVar Miner

List of variants in gene CRYAA reported as benign for cataract 9 multiple types

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000394.4(CRYAA):c.6C>T (p.Asp2=) rs872331 0.60786
NM_000394.4(CRYAA):c.*507C>G rs79614970 0.09429
NM_000394.4(CRYAA):c.*93T>G rs112855370 0.07095
NM_000394.4(CRYAA):c.444T>A (p.Thr148=) rs61735857 0.03116
NM_000394.4(CRYAA):c.327C>T (p.Tyr109=) rs79100529 0.01190
NM_000394.4(CRYAA):c.246G>A (p.Pro82=) rs61735856 0.01115
NM_000394.4(CRYAA):c.54C>T (p.Tyr18=) rs61729442 0.00859
NM_000394.4(CRYAA):c.324C>T (p.Gly108=) rs113802426 0.00399
NM_000394.4(CRYAA):c.*485G>A rs13048089
NM_000394.4(CRYAA):c.213C>T (p.Phe71=)

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.