ClinVar Miner

List of variants in gene ALAD 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: 11
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HGVS dbSNP
NM_000031.6(ALAD):c.*1811_*1812del rs142213018
NM_000031.6(ALAD):c.*613G>A rs818707
NM_000031.6(ALAD):c.*871C>A rs8177822
NM_000031.6(ALAD):c.177G>C (p.Lys59Asn) rs1800435
NM_000031.6(ALAD):c.397+12C>T rs8177805
NM_000031.6(ALAD):c.414C>T (p.Asn138=) rs2228083
NM_000031.6(ALAD):c.463T>C (p.Leu155=) rs8177807
NM_001003945.2(ALAD):c.-234C>G rs7026518
NM_001003945.2(ALAD):c.-234dup rs143518565
NM_001003945.2(ALAD):c.-235_-234dup rs143518565
NM_001003945.2(ALAD):c.-256C>T rs28550589

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