List of variants in gene NHLRC1 reported as likely benign by GeneDx

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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_198586.3(NHLRC1):c.*237T>C	rs73379118	0.01527
NM_198586.3(NHLRC1):c.*85T>A	rs73379121	0.01526
NM_198586.3(NHLRC1):c.*276G>C	rs11966748	0.01453
NC_000006.12:g.18122937A>G	rs114220157	0.00824
NC_000006.12:g.18122700G>C	rs150384028	0.00664
NM_198586.3(NHLRC1):c.*344A>T	rs147528518	0.00663
NM_198586.3(NHLRC1):c.*320G>A	rs79197160	0.00352
NM_198586.3(NHLRC1):c.32C>A (p.Ala11Glu)	rs139029314	0.00181
NM_198586.3(NHLRC1):c.46A>G (p.Met16Val)	rs146636139	0.00108
NM_198586.3(NHLRC1):c.977C>A (p.Thr326Asn)	rs770587249	0.00013
NM_198586.3(NHLRC1):c.1091C>T (p.Ser364Leu)	rs78324544	0.00009
NM_198586.3(NHLRC1):c.933G>T (p.Gly311=)	rs527299943	0.00008
NM_198586.3(NHLRC1):c.1092G>A (p.Ser364=)	rs760322295	0.00005
NM_198586.3(NHLRC1):c.642A>G (p.Gln214=)	rs754756237	0.00005
NM_198586.3(NHLRC1):c.111G>A (p.Gln37=)	rs143893542	0.00002
NM_198586.3(NHLRC1):c.285A>G (p.Ser95=)	rs1057521817	0.00001
NM_198586.3(NHLRC1):c.1072A>C (p.Met358Leu)	rs765443391
NM_198586.3(NHLRC1):c.1185G>A (p.Gly395=)	rs760726977
NM_198586.3(NHLRC1):c.831G>C (p.Ala277=)	rs556216487

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.