List of variants in gene NLRP7 reported as benign for trophoblastic neoplasm

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001127255.2(NLRP7):c.390G>A (p.Gln130=)	rs775883	0.39585
NM_001127255.2(NLRP7):c.-39-16C>T	rs775886	0.38318
NM_001127255.2(NLRP7):c.955G>A (p.Val319Ile)	rs775882	0.29687
NM_001127255.2(NLRP7):c.1460G>A (p.Gly487Glu)	rs775881	0.13795
NM_001127255.2(NLRP7):c.1441G>A (p.Ala481Thr)	rs61747414	0.11267
NM_001127255.2(NLRP7):c.1532A>G (p.Lys511Arg)	rs61743949	0.03179
NM_001127255.2(NLRP7):c.1137G>A (p.Lys379=)	rs10418277
NM_001127255.2(NLRP7):c.1491C>T (p.Ile497=)	rs775880

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.