ClinVar Miner

List of variants in gene MARVELD2 reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001038603.3(MARVELD2):c.176C>T (p.Pro59Leu) rs150434290 0.00053
NM_001038603.3(MARVELD2):c.1033A>G (p.Met345Val) rs142560436 0.00030
NM_001038603.3(MARVELD2):c.585A>G (p.Ile195Met) rs144870558 0.00029
NM_001038603.3(MARVELD2):c.*2G>A rs530892254 0.00017
NM_001038603.3(MARVELD2):c.1310T>C (p.Ile437Thr) rs140452135 0.00016
NM_001038603.3(MARVELD2):c.868C>T (p.Pro290Ser) rs757498916 0.00014
NM_001038603.3(MARVELD2):c.288C>A (p.Asp96Glu) rs73113102 0.00008
NM_001038603.3(MARVELD2):c.1006C>T (p.Arg336Trp) rs779060557 0.00006
NM_001038603.3(MARVELD2):c.115C>T (p.Arg39Trp) rs145027254 0.00006
NM_001038603.3(MARVELD2):c.1438C>G (p.Leu480Val) rs767671073 0.00005
NM_001038603.3(MARVELD2):c.1461T>G (p.Asp487Glu) rs727503161 0.00003
NM_001038603.3(MARVELD2):c.*1C>T rs570049997 0.00002
NM_001038603.3(MARVELD2):c.1147-2A>G rs763062791 0.00001
NM_001038603.3(MARVELD2):c.1204G>A (p.Asp402Asn) rs727503160 0.00001
NM_001038603.3(MARVELD2):c.1286C>T (p.Pro429Leu) rs1554047535
NM_001038603.3(MARVELD2):c.919G>A (p.Ala307Thr) rs779068129

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.