ClinVar Miner

List of variants studied for premature ovarian failure 1 by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (4):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002024.6(FMR1):c.414G>A (p.Arg138=)	rs25707	0.10515
NM_002024.6(FMR1):c.433G>T (p.Ala145Ser)	rs29281	0.02758
NM_002024.6(FMR1):c.18G>T (p.Val6=)	rs111485627	0.00830
NM_002024.6(FMR1):c.1580G>A (p.Arg527His)	rs782738200	0.00001

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.