ClinVar Miner

List of variants in gene MAX studied for cardiovascular organ benign neoplasm

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP
NM_002382.5(MAX):c.*1023C>T rs886050629
NM_002382.5(MAX):c.*1123A>C rs552459072
NM_002382.5(MAX):c.*1127G>C rs4902357
NM_002382.5(MAX):c.*1229C>T rs562514408
NM_002382.5(MAX):c.*1276G>C rs748335228
NM_002382.5(MAX):c.*1278C>T rs541851564
NM_002382.5(MAX):c.*1285T>C rs886050628
NM_002382.5(MAX):c.*1308C>T rs527697025
NM_002382.5(MAX):c.*144C>T rs191382960
NM_002382.5(MAX):c.*170C>T rs762709691
NM_002382.5(MAX):c.*248A>T rs559154342
NM_002382.5(MAX):c.*297C>T rs561525266
NM_002382.5(MAX):c.*320T>G rs750680125
NM_002382.5(MAX):c.*344T>A rs561238353
NM_002382.5(MAX):c.*375G>A rs539220905
NM_002382.5(MAX):c.*404C>T rs4902359
NM_002382.5(MAX):c.*405G>A rs45440292
NM_002382.5(MAX):c.*44G>A rs767990726
NM_002382.5(MAX):c.*461C>T rs183428804
NM_002382.5(MAX):c.*503T>G rs886050633
NM_002382.5(MAX):c.*534G>A rs886050632
NM_002382.5(MAX):c.*565G>A rs1957948
NM_002382.5(MAX):c.*587G>A rs1957949
NM_002382.5(MAX):c.*603C>G rs117802316
NM_002382.5(MAX):c.*608_*609CA[1] rs886050631
NM_002382.5(MAX):c.*717T>C rs4902358
NM_002382.5(MAX):c.*7C>T rs199514174
NM_002382.5(MAX):c.*873T>C rs183467855
NM_002382.5(MAX):c.*92G>A rs45604339
NM_002382.5(MAX):c.*942C>T rs886050630
NM_002382.5(MAX):c.-100T>G rs111941208
NM_002382.5(MAX):c.-110A>T rs886050636
NM_002382.5(MAX):c.-126_-123AGTG[4] rs556734672
NM_002382.5(MAX):c.-126_-123AGTG[6] rs556734672
NM_002382.5(MAX):c.-127G>A rs886050637
NM_002382.5(MAX):c.-152_-151TG[8] rs886050638
NM_002382.5(MAX):c.-18C>T rs201456746
NM_002382.5(MAX):c.-30C>G rs755465193
NM_002382.5(MAX):c.-80G>A rs886050634
NM_002382.5(MAX):c.-94G>C rs536235832
NM_002382.5(MAX):c.-98G>T rs556543602
NM_002382.5(MAX):c.-99G>A rs570017996
NM_002382.5(MAX):c.25G>T (p.Val9Leu) rs201743423
NM_002382.5(MAX):c.37-25dup rs747340873

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