List of variants reported as uncertain significance for Primary dilated cardiomyopathy by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 40

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014391.3(ANKRD1):c.*319A>G	rs142439928	0.00587
NM_014391.3(ANKRD1):c.*343A>G	rs41286920	0.00174
NM_014391.2(ANKRD1):c.-79C>T	rs369861544	0.00095
NM_014391.3(ANKRD1):c.197G>A (p.Arg66Gln)	rs150797476	0.00092
NM_014391.3(ANKRD1):c.369G>A (p.Thr123=)	rs148979787	0.00069
NM_014391.3(ANKRD1):c.313C>T (p.Pro105Ser)	rs148189486	0.00037
NM_014391.3(ANKRD1):c.368C>T (p.Thr123Met)	rs145387010	0.00030
NM_014391.3(ANKRD1):c.*642G>A	rs184423047	0.00027
NM_014391.2(ANKRD1):c.-167C>T	rs568634889	0.00021
NM_014391.3(ANKRD1):c.*489G>A	rs192827821	0.00013
NM_014391.2(ANKRD1):c.-102C>T	rs549813663	0.00010
NM_014391.2(ANKRD1):c.-131C>T	rs538475043	0.00010
NM_000116.5(TAFAZZIN):c.*618A>G	rs781924638	0.00007
NM_014391.3(ANKRD1):c.544C>T (p.Arg182Cys)	rs754717867	0.00006
NM_014391.3(ANKRD1):c.821A>G (p.Tyr274Cys)	rs374486076	0.00004
NM_014391.3(ANKRD1):c.881A>G (p.His294Arg)	rs754657888	0.00004
NM_000116.5(TAFAZZIN):c.761C>T (p.Ala254Val)	rs200909606	0.00003
NM_014391.3(ANKRD1):c.*627A>G	rs886047475	0.00003
NM_000116.5(TAFAZZIN):c.*33G>A	rs782129745	0.00002
NM_000116.5(TAFAZZIN):c.270G>A (p.Leu90=)	rs781986219	0.00002
NM_000116.5(TAFAZZIN):c.351G>A (p.Lys117=)	rs782564325	0.00002
NM_014391.3(ANKRD1):c.909C>T (p.Phe303=)	rs765093690	0.00002
NM_000116.5(TAFAZZIN):c.535C>G (p.Pro179Ala)	rs397515744	0.00001
NM_014391.3(ANKRD1):c.3G>C (p.Met1Ile)	rs188706671	0.00001
NM_014391.3(ANKRD1):c.560C>T (p.Ser187Phe)	rs397517251	0.00001
NM_014391.3(ANKRD1):c.943C>T (p.Arg315Cys)	rs775584071	0.00001
NM_000116.5(TAFAZZIN):c.*165T>A	rs2068620449
NM_000116.5(TAFAZZIN):c.*387C>T	rs1057515819
NM_000116.5(TAFAZZIN):c.*648A>C	rs1413243483
NM_000116.5(TAFAZZIN):c.49T>C (p.Trp17Arg)	rs2068313278
NM_000116.5(TAFAZZIN):c.504G>A (p.Lys168=)	rs1057515818
NM_000116.5(TAFAZZIN):c.647-6C>T	rs901353067
NM_014391.2(ANKRD1):c.-131C>G	rs538475043
NM_014391.3(ANKRD1):c.*286C>T	rs886047479
NM_014391.3(ANKRD1):c.*371T>G	rs531523887
NM_014391.3(ANKRD1):c.*607C>A	rs146219881
NM_014391.3(ANKRD1):c.*634G>A	rs1301081047
NM_014391.3(ANKRD1):c.222dup (p.Leu75fs)	rs776659587
NM_014391.3(ANKRD1):c.55G>C (p.Glu19Gln)	rs886047480
NM_014391.3(ANKRD1):c.798G>C (p.Lys266Asn)	rs1847359872

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.