List of variants in gene MAX reported as uncertain significance 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: 37

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HGVS	dbSNP	gnomAD frequency
NM_002382.5(MAX):c.*1229C>T	rs562514408	0.00066
NM_002382.5(MAX):c.*1308C>T	rs527697025	0.00024
NM_002382.5(MAX):c.*873T>C	rs183467855	0.00019
NM_002382.5(MAX):c.*1278C>T	rs541851564	0.00017
NM_002382.5(MAX):c.*1276G>C	rs748335228	0.00013
NM_002382.5(MAX):c.*503T>G	rs886050633	0.00013
NM_002382.5(MAX):c.341A>C (p.Asn114Thr)	rs772912674	0.00012
NM_002382.5(MAX):c.*320T>G	rs750680125	0.00006
NM_002382.5(MAX):c.*534G>A	rs886050632	0.00006
NM_002382.5(MAX):c.*942C>T	rs886050630	0.00004
NM_002382.5(MAX):c.56A>T (p.Gln19Leu)	rs200547781	0.00004
NM_002382.5(MAX):c.*170C>T	rs762709691	0.00003
NM_002382.5(MAX):c.-127G>A	rs886050637	0.00003
NM_002382.5(MAX):c.*1035C>T	rs1357628064	0.00002
NM_002382.5(MAX):c.*943G>A	rs111875569	0.00002
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.*1285T>C	rs886050628	0.00001
NM_002382.5(MAX):c.299G>A (p.Arg100His)	rs776978293	0.00001
NM_002382.5(MAX):c.344A>G (p.Tyr115Cys)	rs769555911	0.00001
NM_002382.5(MAX):c.410G>A (p.Gly137Asp)	rs771696396	0.00001
NM_002382.5(MAX):c.425C>T (p.Ser142Leu)	rs760147253	0.00001
NM_002382.5(MAX):c.466C>T (p.Arg156Trp)	rs768360710	0.00001
NM_002382.5(MAX):c.*1023C>T	rs886050629
NM_002382.5(MAX):c.*169T>C	rs567680521
NM_002382.5(MAX):c.*608CA[1]	rs886050631
NM_002382.5(MAX):c.*678C>T	rs934021031
NM_002382.5(MAX):c.*96C>G	rs949792280
NM_002382.5(MAX):c.-152TG[8]	rs886050638
NM_002382.5(MAX):c.196A>G (p.Lys66Glu)
NM_002382.5(MAX):c.266A>C (p.Lys89Thr)
NM_002382.5(MAX):c.357C>A (p.Asp119Glu)
NM_002382.5(MAX):c.37-15dup	rs747340873
NM_002382.5(MAX):c.373A>C (p.Asn125His)	rs2063062933
NM_002382.5(MAX):c.406G>C (p.Gly136Arg)	rs140490467
NM_002382.5(MAX):c.413C>T (p.Ser138Leu)	rs1176118785
NR_073138.1(MAX):n.146C>G	rs899541680

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