ClinVar Miner

List of variants in gene UMOD reported as benign 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: 13
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HGVS dbSNP
NM_003361.3(UMOD):c.*104C>T rs111699931
NM_003361.3(UMOD):c.*130C>T rs113468667
NM_003361.3(UMOD):c.-47T>C rs75645968
NM_003361.3(UMOD):c.-56G>A rs79245268
NM_003361.3(UMOD):c.1372G>T (p.Val458Leu) rs55772253
NM_003361.3(UMOD):c.1458C>T (p.Tyr486=) rs141800038
NM_003361.3(UMOD):c.264C>T (p.Gly88=) rs77875418
NM_003361.3(UMOD):c.425G>A (p.Arg142Gln) rs199835347
NM_003361.3(UMOD):c.522C>T (p.Cys174=) rs7193058
NM_003361.3(UMOD):c.538C>G (p.Leu180Val) rs187555378
NM_003361.3(UMOD):c.792G>A (p.Val264=) rs13335818
NM_003361.3(UMOD):c.840C>T (p.Pro280=) rs78691203
NM_003361.3(UMOD):c.885G>A (p.Gly295=) rs28544423

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