ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_000518.4(HBB):c.208G>A (p.Gly70Ser) rs33947415
NM_000518.5(HBB):c.-106G>C rs63750681
NM_000518.5(HBB):c.-133G>A rs72561473
NM_000518.5(HBB):c.-15C>A rs193922550
NM_000518.5(HBB):c.-25T>C rs886039874
NM_000518.5(HBB):c.-31C>T rs63750628
NM_000518.5(HBB):c.-51T>C rs386134236
NM_000518.5(HBB):c.-92C>G rs397515291
NM_000518.5(HBB):c.93-23T>C rs111851677

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