ClinVar Miner

List of variants in gene ALDH7A1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_001182.5(ALDH7A1):c.914-102_914-101insC rs796797237 0.01884
NM_001182.4(ALDH7A1):c.-300T>A rs35569843 0.01564
NM_001182.5(ALDH7A1):c.1490-47A>G rs7719091 0.01494
NM_001182.5(ALDH7A1):c.1566-156del rs138464455 0.01336
NM_001182.5(ALDH7A1):c.1094-183G>A rs76737912 0.01133
NM_001182.5(ALDH7A1):c.1415+36C>G rs7737529 0.01133
NM_001182.5(ALDH7A1):c.913+139A>T rs115577885 0.00926
NM_001182.5(ALDH7A1):c.872-192T>C rs370126778 0.00739
NM_001182.4(ALDH7A1):c.-117G>T rs146562077 0.00663
NM_001182.5(ALDH7A1):c.312+95G>A rs77048751 0.00569
NM_001182.5(ALDH7A1):c.*325A>G rs55923017 0.00504
NM_001182.5(ALDH7A1):c.914-266A>G rs114385171 0.00471
NM_001182.5(ALDH7A1):c.1093+270G>A rs77057701 0.00463
NM_001182.5(ALDH7A1):c.1567A>G (p.Thr523Ala) rs61757684 0.00449
NM_001182.5(ALDH7A1):c.696-56T>C rs180985029 0.00439
NM_001182.5(ALDH7A1):c.650+198G>A rs571299453 0.00426
NM_001182.5(ALDH7A1):c.1318-166A>G rs140294186 0.00346
NM_001182.5(ALDH7A1):c.650+156T>C rs538628836 0.00262
NM_001182.4(ALDH7A1):c.-34G>C rs140627539 0.00261
NM_001182.5(ALDH7A1):c.615C>T (p.Asn205=) rs369380330 0.00042
NM_001182.5(ALDH7A1):c.858G>A (p.Val286=) rs150623275 0.00028
NM_001182.5(ALDH7A1):c.39A>G (p.Ala13=) rs201566142 0.00020
NM_001182.5(ALDH7A1):c.246+6A>T rs759910341 0.00018
NM_001182.5(ALDH7A1):c.63T>C (p.Pro21=) rs368427726 0.00014
NM_001182.5(ALDH7A1):c.960C>T (p.Phe320=) rs114516357 0.00014
NM_001182.5(ALDH7A1):c.552C>T (p.Pro184=) rs369859575 0.00013
NM_001182.5(ALDH7A1):c.1305C>G (p.Val435=) rs142975776 0.00010
NM_001182.5(ALDH7A1):c.1201-8T>C rs558579795 0.00008
NM_001182.5(ALDH7A1):c.882G>C (p.Leu294=) rs751053781 0.00005
NM_001182.5(ALDH7A1):c.1068G>A (p.Gln356=) rs376004978 0.00004
NM_001182.5(ALDH7A1):c.720C>T (p.Asp240=) rs757704473 0.00004
NM_001182.5(ALDH7A1):c.1489+4C>T rs775065938 0.00003
NM_001182.5(ALDH7A1):c.354C>T (p.Gly118=) rs149228266 0.00003
NM_001182.5(ALDH7A1):c.1176T>C (p.Gly392=) rs935431600 0.00001
NM_001182.5(ALDH7A1):c.621C>T (p.Ile207=) rs758236544 0.00001
NM_001182.5(ALDH7A1):c.871+7G>A rs201353024 0.00001
NM_001182.5(ALDH7A1):c.1009-245_1009-241dup rs35367836
NM_001182.5(ALDH7A1):c.1009-245_1009-243dup rs35367836
NM_001182.5(ALDH7A1):c.1094-215A>G rs74506530
NM_001182.5(ALDH7A1):c.1200+74G>C rs140989373
NM_001182.5(ALDH7A1):c.129A>G (p.Lys43=) rs1581409165
NM_001182.5(ALDH7A1):c.1489+116del rs201058790
NM_001182.5(ALDH7A1):c.1565+167del rs149432753
NM_001182.5(ALDH7A1):c.1566-228del rs200634440
NM_001182.5(ALDH7A1):c.201G>T (p.Thr67=) rs747643987
NM_001182.5(ALDH7A1):c.393+94del rs199930619
NM_001182.5(ALDH7A1):c.394-332G>T rs552918715
NM_001182.5(ALDH7A1):c.394-59_394-55del rs147659515
NM_001182.5(ALDH7A1):c.518-81_518-75del rs536817740
NM_001182.5(ALDH7A1):c.651-25_651-20del rs781687339
NM_001182.5(ALDH7A1):c.914-101del rs759132307
NM_001182.5(ALDH7A1):c.914-94_914-89del rs201981205

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