ClinVar Miner

List of variants in gene combination LOC100506321, MAX 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: 2
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HGVS dbSNP
NM_002382.5(MAX):c.102A>G (p.Lys34=) rs1060503836
NM_002382.5(MAX):c.87T>C (p.Asn29=) rs771488967

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