ClinVar Miner

List of variants in gene HOGA1 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: 55
Download table as spreadsheet
HGVS dbSNP
NM_138413.4(HOGA1):c.*101C>T rs41290458
NM_138413.4(HOGA1):c.*1047T>C rs537101942
NM_138413.4(HOGA1):c.*1059A>C rs886047524
NM_138413.4(HOGA1):c.*186C>A rs576078709
NM_138413.4(HOGA1):c.*186C>T rs576078709
NM_138413.4(HOGA1):c.*204T>A rs886047519
NM_138413.4(HOGA1):c.*288A>C rs886047520
NM_138413.4(HOGA1):c.*289C>T rs540860054
NM_138413.4(HOGA1):c.*290G>A rs144890621
NM_138413.4(HOGA1):c.*292C>T rs771988623
NM_138413.4(HOGA1):c.*350dup rs1554875325
NM_138413.4(HOGA1):c.*352T>C rs545072905
NM_138413.4(HOGA1):c.*353_*354dup rs5787248
NM_138413.4(HOGA1):c.*354dup rs5787248
NM_138413.4(HOGA1):c.*359dup rs561998392
NM_138413.4(HOGA1):c.*381_*382AG[1] rs886047523
NM_138413.4(HOGA1):c.*425T>C rs189957405
NM_138413.4(HOGA1):c.*485C>T rs553100036
NM_138413.4(HOGA1):c.*733C>T rs764120248
NM_138413.4(HOGA1):c.*850G>T rs560555907
NM_138413.4(HOGA1):c.*950G>A rs190392004
NM_138413.4(HOGA1):c.110G>T (p.Gly37Val) rs772722925
NM_138413.4(HOGA1):c.185A>T (p.His62Leu) rs150812556
NM_138413.4(HOGA1):c.208C>T (p.Arg70Ter) rs758304537
NM_138413.4(HOGA1):c.212-21A>G rs11817730
NM_138413.4(HOGA1):c.212-6T>C rs372066473
NM_138413.4(HOGA1):c.221T>G (p.Val74Gly) rs796052084
NM_138413.4(HOGA1):c.22_24TCT[1] (p.Ser9del) rs1554872338
NM_138413.4(HOGA1):c.289C>T (p.Arg97Cys) rs267606762
NM_138413.4(HOGA1):c.337G>A (p.Glu113Lys) rs150702945
NM_138413.4(HOGA1):c.341-82del rs796052083
NM_138413.4(HOGA1):c.396G>A (p.Ala132=) rs41290456
NM_138413.4(HOGA1):c.398C>T (p.Ala133Val) rs374367160
NM_138413.4(HOGA1):c.39G>A (p.Gly13=) rs200127255
NM_138413.4(HOGA1):c.469-13C>T rs750664684
NM_138413.4(HOGA1):c.469-25C>T rs7078003
NM_138413.4(HOGA1):c.469-31C>T rs75929214
NM_138413.4(HOGA1):c.529G>T (p.Asp177Tyr) rs777601935
NM_138413.4(HOGA1):c.535C>A (p.Pro179Thr) rs374327791
NM_138413.4(HOGA1):c.538G>A (p.Val180Met) rs114177505
NM_138413.4(HOGA1):c.634A>G (p.Thr212Ala) rs779492256
NM_138413.4(HOGA1):c.700+67G>A rs2297643
NM_138413.4(HOGA1):c.700+7C>T rs57616820
NM_138413.4(HOGA1):c.700+9C>T rs375091787
NM_138413.4(HOGA1):c.701-18G>C rs201596675
NM_138413.4(HOGA1):c.713del (p.Gly238fs) rs760930050
NM_138413.4(HOGA1):c.745C>G (p.Gln249Glu) rs368276974
NM_138413.4(HOGA1):c.752G>C (p.Cys251Ser) rs886047518
NM_138413.4(HOGA1):c.828C>T (p.Asn276=) rs201683794
NM_138413.4(HOGA1):c.834+42G>T rs115279832
NM_138413.4(HOGA1):c.872T>C (p.Ile291Thr) rs1554875257
NM_138413.4(HOGA1):c.910G>A (p.Ala304Thr) rs116527624
NM_138413.4(HOGA1):c.912C>A (p.Ala304=) rs12261752
NM_138413.4(HOGA1):c.91_93AAG[1] (p.Lys32del) rs750736378
NM_138413.4(HOGA1):c.943_954dup (p.Glu315_Arg318dup) rs777828182

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.