ClinVar Miner

List of variants in gene LOC130055850, MAX studied for benign neoplasm

Included ClinVar conditions (127):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_002382.5(MAX):c.-100T>G rs111941208 0.00769
NM_002382.5(MAX):c.-94G>C rs536235832 0.00379
NM_002382.5(MAX):c.-18C>T rs201456746 0.00027
NM_002382.5(MAX):c.-80G>A rs886050634 0.00022
NM_002382.5(MAX):c.-98G>T rs556543602 0.00014
NM_002382.5(MAX):c.25G>T (p.Val9Leu) rs201743423 0.00007
NM_002382.5(MAX):c.-30C>G rs755465193 0.00003
NM_002382.5(MAX):c.-110A>T rs886050636
NM_002382.5(MAX):c.-126AGTG[4] rs556734672
NM_002382.5(MAX):c.-126AGTG[6] rs556734672
NM_002382.5(MAX):c.-99G>A rs570017996

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