ClinVar Miner

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

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP
NM_002382.4(MAX):c.37-15dupT rs747340873
NM_002382.5(MAX):c.*1023C>T rs886050629
NM_002382.5(MAX):c.*1276G>C rs748335228
NM_002382.5(MAX):c.*1285T>C rs886050628
NM_002382.5(MAX):c.*170C>T rs762709691
NM_002382.5(MAX):c.*320T>G rs750680125
NM_002382.5(MAX):c.*44G>A rs767990726
NM_002382.5(MAX):c.*503T>G rs886050633
NM_002382.5(MAX):c.*534G>A rs886050632
NM_002382.5(MAX):c.*608_*609CA[1] rs886050631
NM_002382.5(MAX):c.*942C>T rs886050630
NM_002382.5(MAX):c.-110A>T rs886050636
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.-30C>G rs755465193
NM_002382.5(MAX):c.-80G>A rs886050634
NM_002382.5(MAX):c.21C>G (p.Ile7Met) rs760248675
NM_002382.5(MAX):c.25G>T (p.Val9Leu) rs201743423
NM_002382.5(MAX):c.268C>T (p.Arg90Trp) rs1060500099
NM_002382.5(MAX):c.277G>C (p.Ala93Pro) rs1555340540
NM_002382.5(MAX):c.284T>C (p.Leu95Pro) rs878854499
NM_002382.5(MAX):c.285G>A (p.Leu95=) rs878854500
NM_002382.5(MAX):c.295+6C>T rs146552320
NM_002382.5(MAX):c.296-1G>A rs1555340265
NM_002382.5(MAX):c.298C>T (p.Arg100Cys) rs762084527
NM_002382.5(MAX):c.299G>A (p.Arg100His)
NM_002382.5(MAX):c.308A>G (p.Glu103Gly)
NM_002382.5(MAX):c.314C>T (p.Ala105Val) rs769051095
NM_002382.5(MAX):c.329A>C (p.Gln110Pro) rs775808138
NM_002382.5(MAX):c.331C>G (p.Leu111Val) rs748675729
NM_002382.5(MAX):c.337A>T (p.Thr113Ser) rs1060500100
NM_002382.5(MAX):c.341A>C (p.Asn114Thr) rs772912674
NM_002382.5(MAX):c.346C>G (p.Pro116Ala)
NM_002382.5(MAX):c.359A>G (p.Asn120Ser) rs80206158
NM_002382.5(MAX):c.360C>A (p.Asn120Lys) rs1555340209
NM_002382.5(MAX):c.376G>A (p.Ala126Thr)
NM_002382.5(MAX):c.388A>G (p.Thr130Ala) rs1566598180
NM_002382.5(MAX):c.397G>A (p.Ala133Thr) rs750459929
NM_002382.5(MAX):c.403G>C (p.Asp135His)
NM_002382.5(MAX):c.406G>A (p.Gly136Arg) rs140490467
NM_002382.5(MAX):c.410G>A (p.Gly137Asp)
NM_002382.5(MAX):c.414G>A (p.Ser138=) rs559090673
NM_002382.5(MAX):c.415G>A (p.Asp139Asn) rs772397458
NM_002382.5(MAX):c.41A>G (p.Glu14Gly) rs876660888
NM_002382.5(MAX):c.425C>T (p.Ser142Leu) rs760147253
NM_002382.5(MAX):c.442dup (p.Glu148fs) rs1566597938
NM_002382.5(MAX):c.466C>T (p.Arg156Trp)
NM_002382.5(MAX):c.467G>A (p.Arg156Gln) rs876659544
NM_002382.5(MAX):c.56A>T (p.Gln19Leu) rs200547781

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.