ClinVar Miner

List of variants in gene ZNF423 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: 25
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HGVS dbSNP
NM_001271620.2(ZNF423):c.108C>T (p.Asp36=) rs117266679
NM_001271620.2(ZNF423):c.1122G>A (p.Ala374=) rs16947743
NM_001271620.2(ZNF423):c.1356C>T (p.Asp452=) rs149371639
NM_001271620.2(ZNF423):c.1365T>C (p.Asn455=) rs13336762
NM_001271620.2(ZNF423):c.1665G>A (p.Pro555=) rs16947741
NM_001271620.2(ZNF423):c.1706A>G (p.Asn569Ser) rs34214571
NM_001271620.2(ZNF423):c.1782C>T (p.His594=) rs75294107
NM_001271620.2(ZNF423):c.1809G>A (p.Ala603=) rs143468235
NM_001271620.2(ZNF423):c.1929G>A (p.Ser643=) rs143934881
NM_001271620.2(ZNF423):c.2124C>T (p.His708=) rs73565356
NM_001271620.2(ZNF423):c.2331C>T (p.Thr777=) rs77996576
NM_001271620.2(ZNF423):c.2358C>A (p.Pro786=) rs12599354
NM_001271620.2(ZNF423):c.2857C>T (p.Leu953=) rs35529066
NM_001271620.2(ZNF423):c.2960C>T (p.Ala987Val) rs111229124
NM_001271620.2(ZNF423):c.2976G>A (p.Ala992=) rs117592972
NM_001271620.2(ZNF423):c.3022C>A (p.Leu1008Met) rs79706004
NM_001271620.2(ZNF423):c.3087C>T (p.Tyr1029=) rs150027129
NM_001271620.2(ZNF423):c.3132G>A (p.Val1044=) rs61739947
NM_001271620.2(ZNF423):c.3147G>A (p.Pro1049=) rs113531514
NM_001271620.2(ZNF423):c.3157G>A (p.Ala1053Thr) rs147898137
NM_001271620.2(ZNF423):c.3189C>T (p.Pro1063=) rs61755180
NM_001271620.2(ZNF423):c.3646-9C>T rs78514142
NM_001271620.2(ZNF423):c.507C>T (p.Arg169=) rs16947744
NM_001271620.2(ZNF423):c.603C>T (p.Asp201=) rs145503941
NM_001271620.2(ZNF423):c.990G>A (p.Pro330=) rs61747467

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