List of variants in gene LPIN1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001349206.2(LPIN1):c.*1082del	rs147471777	0.01970
NM_001349206.2(LPIN1):c.1729A>G (p.Ile577Val)	rs148499322	0.00173
NM_001349206.2(LPIN1):c.*1656G>C	rs532325743	0.00170
NM_001349206.2(LPIN1):c.*2208T>C	rs187949091	0.00131
NM_001349206.2(LPIN1):c.*2082C>T	rs182433960	0.00109
NM_001349206.2(LPIN1):c.*1604T>C	rs534753112	0.00044
NM_001349206.2(LPIN1):c.*2274C>G	rs184826929	0.00039
NM_001349206.2(LPIN1):c.1242G>A (p.Thr414=)	rs370978470	0.00005
NM_001349206.2(LPIN1):c.*1933G>C	rs148741595
NM_001349206.2(LPIN1):c.958TCT[2] (p.Ser322del)	rs149564563

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.