ClinVar Miner

List of variants in gene APOA1 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: 6
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HGVS dbSNP
NM_000039.2(APOA1):c.116C>T (p.Ala39Val) rs746314593
NM_000039.2(APOA1):c.168G>A (p.Gln56=) rs760886281
NM_000039.2(APOA1):c.28G>A (p.Val10Met) rs750125257
NM_000039.2(APOA1):c.480G>T (p.Glu160Asp) rs769548576
NM_000039.2(APOA1):c.498C>A (p.Ser166Arg) rs757899657
NM_000039.2(APOA1):c.9T>C (p.Ala3=) rs141383703

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