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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_002382.5(MAX):c.*587G>A	rs1957949	0.52668
NM_002382.5(MAX):c.*565G>A	rs1957948	0.48891
NM_002382.5(MAX):c.*1127G>C	rs4902357	0.48713
NM_002382.5(MAX):c.*404C>T	rs4902359	0.48552
NM_002382.5(MAX):c.*717T>C	rs4902358	0.27135
NM_002382.5(MAX):c.*92G>A	rs45604339	0.26844
NM_002382.5(MAX):c.*461C>T	rs183428804	0.00262
NM_002382.5(MAX):c.*616C>T	rs192895631	0.00103
NM_002382.5(MAX):c.*7C>T	rs199514174	0.00051
NM_002382.5(MAX):c.*144C>T	rs191382960	0.00050
NM_002382.5(MAX):c.*128T>A	rs539193441	0.00029
NM_002382.5(MAX):c.*1123A>C	rs552459072	0.00014
NM_002382.5(MAX):c.*375G>A	rs539220905	0.00009
NM_002382.5(MAX):c.*248A>T	rs559154342	0.00007
NM_002382.5(MAX):c.*297C>T	rs561525266	0.00007
NM_002382.5(MAX):c.295+10C>T	rs375446224	0.00002
NM_002382.5(MAX):c.*344T>A	rs561238353
NM_002382.5(MAX):c.*65G>C	rs566299166
NM_002382.5(MAX):c.*700G>T	rs139403325

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