ClinVar Miner

List of variants in gene MAX reported as likely benign for benign neoplasm

Included ClinVar conditions (123):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_002382.5(MAX):c.*603C>G rs117802316 0.01457
NM_002382.5(MAX):c.*405G>A rs45440292 0.00825
NM_002382.5(MAX):c.172-6230G>A rs148339628 0.00097
NM_002382.5(MAX):c.406G>A (p.Gly136Arg) rs140490467 0.00019
NM_002382.5(MAX):c.56A>T (p.Gln19Leu) rs200547781 0.00004
NM_002382.5(MAX):c.*44G>A rs767990726 0.00003
NM_002382.5(MAX):c.329A>C (p.Gln110Pro) rs775808138 0.00002
NM_002382.5(MAX):c.397G>A (p.Ala133Thr) rs750459929 0.00002
NM_002382.5(MAX):c.172-6278_172-6277del

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