ClinVar Miner

List of variants in gene ALDH18A1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002860.4(ALDH18A1):c.558+297A>T rs56256708 0.01524
NM_002860.4(ALDH18A1):c.1605+111T>C rs72807340 0.01241
NM_002860.4(ALDH18A1):c.1924-234C>G rs546265 0.01004
NM_002860.4(ALDH18A1):c.1467+245C>T rs191350365 0.00894
NM_002860.4(ALDH18A1):c.89-142A>G rs117819105 0.00836
NM_002860.4(ALDH18A1):c.718-151G>T rs75576572 0.00782
NM_002860.4(ALDH18A1):c.*56T>A rs114393346 0.00549
NM_002860.4(ALDH18A1):c.2207-3C>T rs149309642 0.00472
NM_002860.4(ALDH18A1):c.1605+203C>T rs142553084 0.00445
NM_002860.4(ALDH18A1):c.559-208G>A rs182106689 0.00444
NM_002860.4(ALDH18A1):c.*292C>T rs78053774 0.00329
NM_002860.4(ALDH18A1):c.1152+84A>G rs147367157 0.00322
NM_002860.4(ALDH18A1):c.2232G>A (p.Ser744=) rs148601288 0.00153
NM_002860.4(ALDH18A1):c.-29+10G>A rs571140165 0.00119
NM_002860.4(ALDH18A1):c.1308G>A (p.Leu436=) rs144816455 0.00112
NM_002860.4(ALDH18A1):c.1467+86T>C rs552316778 0.00098
NM_002860.4(ALDH18A1):c.2160C>T (p.Phe720=) rs374052426 0.00070
NM_002860.4(ALDH18A1):c.1314C>T (p.Ile438=) rs150526956 0.00042
NM_002860.4(ALDH18A1):c.*8C>T rs201876082 0.00037
NM_002860.4(ALDH18A1):c.492C>T (p.Ala164=) rs150472102 0.00032
NM_002860.4(ALDH18A1):c.1153-13A>G rs370680325 0.00024
NM_002860.4(ALDH18A1):c.1248G>A (p.Gly416=) rs757733068 0.00009
NM_002860.4(ALDH18A1):c.2110+13A>G rs375782465 0.00007
NM_002860.4(ALDH18A1):c.1596C>T (p.Ala532=) rs200730342 0.00006
NM_002860.4(ALDH18A1):c.2335A>G (p.Ser779Gly) rs143874727 0.00006
NM_002860.4(ALDH18A1):c.1014C>T (p.His338=) rs150056435 0.00004
NM_002860.4(ALDH18A1):c.1078+17A>G rs745857450 0.00004
NM_002860.4(ALDH18A1):c.1368C>T (p.Arg456=) rs369979669 0.00004
NM_002860.4(ALDH18A1):c.240C>T (p.Ala80=) rs1016828034 0.00004
NM_002860.4(ALDH18A1):c.304-3C>T rs188362786 0.00004
NM_002860.4(ALDH18A1):c.1110G>A (p.Ala370=) rs558532112 0.00003
NM_002860.4(ALDH18A1):c.1380C>T (p.Ile460=) rs770247123 0.00003
NM_002860.4(ALDH18A1):c.1467+15C>T rs374652686 0.00003
NM_002860.4(ALDH18A1):c.2040C>T (p.Asn680=) rs145806693 0.00003
NM_002860.4(ALDH18A1):c.2121G>A (p.Ala707=) rs753837028 0.00003
NM_002860.4(ALDH18A1):c.231C>T (p.Leu77=) rs1278292461 0.00002
NM_002860.4(ALDH18A1):c.2361C>T (p.Leu787=) rs377506019 0.00002
NM_002860.4(ALDH18A1):c.966C>T (p.Gly322=) rs754882491 0.00002
NM_002860.4(ALDH18A1):c.-29_-29+1dup rs1064795755 0.00001
NM_002860.4(ALDH18A1):c.1363T>C (p.Leu455=) rs753823851 0.00001
NM_002860.4(ALDH18A1):c.1635T>C (p.Leu545=) rs368774840 0.00001
NM_002860.4(ALDH18A1):c.-120A>G rs181772739
NM_002860.4(ALDH18A1):c.-28-4G>C rs2139670360
NM_002860.4(ALDH18A1):c.-69CG[4] rs200542959
NM_002860.4(ALDH18A1):c.1134C>T (p.Ala378=) rs749391185
NM_002860.4(ALDH18A1):c.1247-70del rs766601424
NM_002860.4(ALDH18A1):c.1467+82dup rs75882174
NM_002860.4(ALDH18A1):c.1606-18del rs532582192
NM_002860.4(ALDH18A1):c.1624G>A (p.Val542Ile) rs552325165
NM_002860.4(ALDH18A1):c.1960C>T (p.Leu654=) rs905973576
NM_002860.4(ALDH18A1):c.2111-7C>A rs542177817
NM_002860.4(ALDH18A1):c.354A>T (p.Gly118=) rs1589544043
NM_002860.4(ALDH18A1):c.945C>T (p.Ala315=) rs566528582

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.