ClinVar Miner

List of variants in gene ALG1 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_019109.5(ALG1):c.740+191C>T rs8054647 0.01556
NM_019109.5(ALG1):c.629+166G>A rs116891668 0.01390
NM_019109.5(ALG1):c.1263+268G>A rs114975301 0.01379
NM_019109.5(ALG1):c.1187+204A>G rs148038550 0.01378
NM_019109.5(ALG1):c.390+46T>A rs111714766 0.01259
NM_019109.5(ALG1):c.391-40G>C rs78146072 0.01213
NM_019109.5(ALG1):c.1073-84G>T rs115290312 0.01134
NM_019109.5(ALG1):c.901+46A>C rs184902380 0.01133
NM_019109.5(ALG1):c.1263+125G>A rs146192049 0.01129
NM_019109.5(ALG1):c.1263+208dup rs111566454 0.00866
NM_019109.5(ALG1):c.539+69A>G rs112042401 0.00860
NM_019109.5(ALG1):c.902-103C>T rs141341385 0.00739
NM_019109.5(ALG1):c.741-89C>A rs112612638 0.00728
NM_019109.5(ALG1):c.962-237C>T rs534464751 0.00681
NM_019109.5(ALG1):c.1072+47T>G rs748636979 0.00659
NM_019109.5(ALG1):c.1080G>A (p.Ala360=) rs143939207 0.00467
NM_019109.5(ALG1):c.539+16G>A rs189715949 0.00311
NM_019109.5(ALG1):c.867C>T (p.Asp289=) rs144029725 0.00265
NM_019109.5(ALG1):c.1092C>G (p.Val364=) rs113602091 0.00221
NM_019109.5(ALG1):c.1222C>T (p.Leu408=) rs149319732 0.00217
NM_019109.5(ALG1):c.21C>T (p.Val7=) rs149388535 0.00093
NM_019109.5(ALG1):c.902-20G>A rs74249172 0.00059
NM_019109.5(ALG1):c.391-15C>G rs374836725 0.00046
NM_019109.5(ALG1):c.540-13T>C rs201477967 0.00023
NM_019109.5(ALG1):c.629+20C>T rs371416008 0.00014
NM_019109.5(ALG1):c.384T>C (p.Phe128=) rs140626461 0.00011
NM_019109.5(ALG1):c.863-15A>G rs371947976 0.00010
NM_019109.5(ALG1):c.286+15A>C rs376062732 0.00006
NM_019109.5(ALG1):c.286+10C>T rs371480769 0.00003
NM_019109.5(ALG1):c.961+19G>A rs768688738 0.00003
NM_019109.5(ALG1):c.579G>A (p.Leu193=) rs750145784 0.00002
NM_019109.5(ALG1):c.391-13C>G rs768190163 0.00001
NM_019109.5(ALG1):c.863-14T>C rs780024263 0.00001
NM_019109.4(ALG1):c.-10G>T rs761476388
NM_019109.4(ALG1):c.93G>A (p.Ala31=) rs1555450976
NM_019109.5(ALG1):c.390+13C>A rs62036244
NM_019109.5(ALG1):c.390+207C>G rs112467044
NM_019109.5(ALG1):c.630-18G>A rs545873278
NM_019109.5(ALG1):c.714C>T (p.Gly238=) rs1057521392
NM_019109.5(ALG1):c.863-15A>C rs371947976
NM_019109.5(ALG1):c.902-47del rs911082490
NM_019109.5(ALG1):c.961+242TTG[2] rs541822791
NM_019109.5(ALG1):c.961+281_961+282dup rs34927441
NM_019109.5(ALG1):c.961+8C>G rs371353008
NM_019109.5(ALG1):c.962-74G>A rs545697245

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