ClinVar Miner

List of variants in gene AHI1 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001134831.2(AHI1):c.1912+135A>G rs2614274 0.98712
NM_001134831.2(AHI1):c.749+215A>G rs2757651 0.97799
NM_001134831.2(AHI1):c.2374-186G>A rs980318 0.97797
NM_001134831.2(AHI1):c.1151+261T>C rs2757648 0.97614
NM_001134831.2(AHI1):c.2267-156A>G rs2614270 0.95577
NM_001134831.2(AHI1):c.-139-114A>G rs9494250 0.89823
NM_001134831.2(AHI1):c.2764+105T>C rs2757639 0.87941
NM_001134831.2(AHI1):c.1780-14C>T rs2757645 0.81825
NM_001134831.2(AHI1):c.2266+235G>A rs2255078 0.76052
NM_001134831.2(AHI1):c.10+115C>A rs9402709 0.73311
NM_001134831.2(AHI1):c.3426+13G>A rs6914831 0.59084
NM_017651.4(AHI1):c.-293G>T rs13197384 0.29491
NM_001134831.2(AHI1):c.*218C>T rs1052502 0.27386
NM_001134831.2(AHI1):c.3485+38G>C rs4896141 0.23072
NM_001134831.2(AHI1):c.3589-106A>G rs11970282 0.11912
NM_001134831.2(AHI1):c.2961+292C>T rs17778438 0.08418
NM_001134831.2(AHI1):c.1441-76T>C rs11964449 0.08151
NM_001134831.2(AHI1):c.3165+42G>C rs7772864 0.06222
NM_001134831.2(AHI1):c.3485+159del rs376389888 0.03622
NM_001134831.2(AHI1):c.-299G>A rs113052089 0.03529
NM_001134831.2(AHI1):c.1913-319G>A rs79218814 0.03437
NM_001134831.2(AHI1):c.2266+120T>C rs78942984 0.03416
NM_001134831.2(AHI1):c.2373+72A>G rs111866629 0.03301
NM_001134831.2(AHI1):c.3329-229T>C rs17064414 0.03072
NM_001134831.2(AHI1):c.2493-243A>G rs147529039 0.02816
NM_001134831.2(AHI1):c.1780-86_1780-83del rs200653130 0.02436
NM_001134831.2(AHI1):c.135+184C>G rs17064588 0.02424
NM_001134831.2(AHI1):c.135+174A>G rs75218524 0.02423
NM_001134831.2(AHI1):c.2223T>C (p.Asp741=) rs2273761 0.02399
NM_001134831.2(AHI1):c.3485+159C>T rs79518333 0.02097
NM_001134831.2(AHI1):c.135+239C>T rs111939059 0.01784
NM_001134831.2(AHI1):c.2624-6A>G rs41288015 0.01635
NM_001134831.2(AHI1):c.2493-123T>A rs116515646 0.01575
NM_001134831.2(AHI1):c.1152-11T>G rs113317693 0.01324
NM_001134831.2(AHI1):c.1643G>A (p.Arg548His) rs35433555 0.01070
NM_001134831.2(AHI1):c.2961+6_2961+7insGAC rs780835322 0.00980
NM_001134831.2(AHI1):c.2962-16A>G rs41287056 0.00707
NM_001134831.2(AHI1):c.3579T>C (p.Thr1193=) rs115338154 0.00537
NM_001134831.2(AHI1):c.3368C>T (p.Ser1123Phe) rs117447608 0.00497
NM_001134831.2(AHI1):c.2798A>G (p.Tyr933Cys) rs41288013 0.00466
NM_001134831.2(AHI1):c.2972G>A (p.Arg991His) rs35851478 0.00429
NM_001134831.2(AHI1):c.2505G>A (p.Arg835=) rs41288017 0.00383
NM_001134831.2(AHI1):c.517G>A (p.Ala173Thr) rs146416468 0.00348
NM_001134831.2(AHI1):c.1791C>T (p.Ile597=) rs150425546 0.00307
NM_001134831.2(AHI1):c.724C>T (p.Pro242Ser) rs143522987 0.00307
NM_001134831.2(AHI1):c.3257A>G (p.Glu1086Gly) rs148000791 0.00115
NM_001134831.2(AHI1):c.*28G>C rs9494209
NM_001134831.2(AHI1):c.-140+191G>A rs6928455
NM_001134831.2(AHI1):c.-202+41C>T rs6570012
NM_001134831.2(AHI1):c.2036+96G>A rs11965621
NM_001134831.2(AHI1):c.2037-77G>A rs737561
NM_001134831.2(AHI1):c.3109+6701dup rs113398452
NM_001134831.2(AHI1):c.3109+7009dup rs376916356
NM_001134831.2(AHI1):c.3110-22_3110-19del rs71725890
NM_001134831.2(AHI1):c.3426+7231G>A
NM_001134831.2(AHI1):c.3427-276dup rs35584012
NM_001134831.2(AHI1):c.3485+159_3485+161del rs1406083848
NM_001134831.2(AHI1):c.3485+174del rs557417336
NM_001134831.2(AHI1):c.3588+210G>A rs73557663

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.