ClinVar Miner

List of variants in gene MAX reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP
NM_002382.5(MAX):c.*1123A>C rs552459072
NM_002382.5(MAX):c.*1127G>C rs4902357
NM_002382.5(MAX):c.*128T>A
NM_002382.5(MAX):c.*144C>T rs191382960
NM_002382.5(MAX):c.*248A>T rs559154342
NM_002382.5(MAX):c.*297C>T rs561525266
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.*461C>T rs183428804
NM_002382.5(MAX):c.*565G>A rs1957948
NM_002382.5(MAX):c.*587G>A rs1957949
NM_002382.5(MAX):c.*616C>T
NM_002382.5(MAX):c.*65G>C
NM_002382.5(MAX):c.*700G>T
NM_002382.5(MAX):c.*717T>C rs4902358
NM_002382.5(MAX):c.*7C>T rs199514174
NM_002382.5(MAX):c.*92G>A rs45604339
NM_002382.5(MAX):c.-100T>G rs111941208
NM_002382.5(MAX):c.-18C>T rs201456746
NM_002382.5(MAX):c.-30C>G rs755465193
NM_002382.5(MAX):c.-94G>C rs536235832
NM_002382.5(MAX):c.-98G>T rs556543602
NM_002382.5(MAX):c.295+10C>T rs375446224

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.