ClinVar Miner

List of variants in gene UMOD reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_003361.3(UMOD):c.*226_*229del rs886051782
NM_003361.3(UMOD):c.*231A>G rs886051781
NM_003361.3(UMOD):c.*59G>A rs886051783
NM_003361.3(UMOD):c.1131G>C (p.Trp377Cys) rs201738891
NM_003361.3(UMOD):c.1177T>C (p.Leu393=) rs748849021
NM_003361.3(UMOD):c.1182+5G>T rs755374625
NM_003361.3(UMOD):c.1680C>G (p.Asp560Glu) rs200473249
NM_003361.3(UMOD):c.1859dup (p.Leu620fs) rs886051784
NM_003361.3(UMOD):c.865+7C>G rs759063012

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