ClinVar Miner

List of variants in gene GATA3 reported as likely 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: 22
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HGVS dbSNP
NM_001002295.2(GATA3):c.*1029C>T rs530772797
NM_001002295.2(GATA3):c.*26C>G rs200946839
NM_001002295.2(GATA3):c.*491A>G rs138815232
NM_001002295.2(GATA3):c.*575A>C rs552915242
NM_001002295.2(GATA3):c.*746C>T rs545858251
NM_001002295.2(GATA3):c.*798G>A rs531077807
NM_001002295.2(GATA3):c.-264G>T rs35971003
NM_001002295.2(GATA3):c.-351C>T rs34628951
NM_001002295.2(GATA3):c.-359G>A rs138512915
NM_001002295.2(GATA3):c.-48G>T rs554517990
NM_001002295.2(GATA3):c.-49C>T rs11567942
NM_001002295.2(GATA3):c.-69G>A rs28395794
NM_001002295.2(GATA3):c.-95G>T rs369825935
NM_001002295.2(GATA3):c.1179C>T (p.Asn393=) rs138679257
NM_001002295.2(GATA3):c.1257G>A (p.Thr419=) rs11567941
NM_001002295.2(GATA3):c.1266G>A (p.Pro422=) rs541782074
NM_001002295.2(GATA3):c.216G>T (p.Val72=) rs560531559
NM_001002295.2(GATA3):c.480C>G (p.Asp160Glu) rs143627754
NM_001002295.2(GATA3):c.573C>T (p.Pro191=) rs35508267
NM_001002295.2(GATA3):c.706C>G (p.Pro236Ala) rs148835259
NM_001002295.2(GATA3):c.72G>A (p.Pro24=) rs202168967
NM_001002295.2(GATA3):c.870C>T (p.Leu290=) rs575091

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