List of variants in gene LDB3, LOC110121486 studied for cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.689+3825G>C	rs3740345	0.66820
NM_001368067.1(LDB3):c.504T>C (p.Asp168=)	rs76615432	0.06909
NM_007078.3(LDB3):c.690-4842G>A	rs113445294	0.06823
NM_001368067.1(LDB3):c.349G>A (p.Asp117Asn)	rs121908338	0.00584
NM_001368067.1(LDB3):c.546T>C (p.Ser182=)	rs71473272	0.00316
NM_001368067.1(LDB3):c.433G>A (p.Gly145Ser)	rs376489385	0.00009
NM_001368067.1(LDB3):c.370C>A (p.Pro124Thr)	rs755513516	0.00005
NM_001368067.1(LDB3):c.333C>G (p.Asn111Lys)	rs369470035	0.00004
NM_001368067.1(LDB3):c.456G>A (p.Ala152=)	rs371708921	0.00002
NM_001368067.1(LDB3):c.430G>A (p.Gly144Ser)	rs915830221	0.00001
NM_001368067.1(LDB3):c.490G>C (p.Asp164His)	rs1000020884	0.00001
NM_001368067.1(LDB3):c.383A>T (p.Lys128Met)	rs121908339
NM_001368067.1(LDB3):c.439G>A (p.Ala147Thr)	rs121908333
NM_001368067.1(LDB3):c.440C>T (p.Ala147Val)	rs281865143
NM_001368067.1(LDB3):c.494C>T (p.Ala165Val)	rs121908334
NM_007078.3(LDB3):c.689+3870C>T	rs1028583921
NM_007078.3(LDB3):c.690-4571A>C	rs111941601

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.