List of variants reported as likely benign for Hyperinsulinemic hypoglycemia

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

Total variants: 24

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_005327.7(HADH):c.-38T>C	rs17550794	0.13430
NM_005327.7(HADH):c.*109T>A	rs221347	0.07950
NM_005327.4(HADH):c.-71C>T	rs760202	0.02129
NM_005327.4(HADH):c.-102G>A	rs182097151	0.00354
NM_005327.7(HADH):c.*377G>A	rs148809781	0.00084
NM_005327.7(HADH):c.*168A>T	rs532458283	0.00062
NM_005327.4(HADH):c.-203A>G	rs376591232	0.00049
NM_005327.7(HADH):c.*142G>A	rs560215584	0.00011
NM_005327.7(HADH):c.827-10C>T	rs372610846	0.00011
NM_005327.7(HADH):c.*305T>A	rs3822294	0.00008
NM_005327.7(HADH):c.240G>A (p.Lys80=)	rs748623569	0.00007
NM_005327.7(HADH):c.*335C>A	rs780532720	0.00006
NM_005327.7(HADH):c.*59G>A	rs529762487	0.00005
NM_005327.7(HADH):c.710-14C>T	rs185267497	0.00004
NM_005327.7(HADH):c.820G>A (p.Val274Met)	rs543440046	0.00004
NM_005327.4(HADH):c.-86G>T	rs528952923	0.00001
NM_005327.7(HADH):c.*279C>A	rs1290272212	0.00001
NM_005327.7(HADH):c.-36C>T	rs746854470	0.00001
NM_005327.7(HADH):c.72G>A (p.Lys24=)	rs781319494	0.00001
NM_005327.4(HADH):c.-193G>T	rs10017687
NM_005327.4(HADH):c.-195A>T	rs886058979
NM_005327.7(HADH):c.132+6C>G	rs772843585
NM_005327.7(HADH):c.21G>A (p.Gln7=)	rs886058980
NM_005327.7(HADH):c.825T>G (p.Asp275Glu)	rs1736344235

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.