ClinVar Miner

List of variants in gene ALG9 reported as benign for ALG9-congenital disorder of glycosylation

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NC_000011.9:g.111742146del rs10708475 1.00000
NM_024740.2(ALG9):c.1602+10449A>G rs610437 0.63674
NM_024740.2(ALG9):c.865G>A (p.Val289Ile) rs10502151 0.28588
NM_024740.2(ALG9):c.*1848G>A rs45620134 0.03051
NM_024740.2(ALG9):c.406-7C>T rs45574638 0.02566
NM_024740.2(ALG9):c.*1671T>C rs116003998 0.01295
NM_024740.2(ALG9):c.764C>T (p.Ser255Leu) rs17113312 0.01232
NM_024740.2(ALG9):c.132-17T>G rs782169051 0.00984
NM_024740.2(ALG9):c.132-13T>G rs72994380 0.00979
NM_024740.2(ALG9):c.1473-14T>C rs187507214 0.00657
NM_024740.2(ALG9):c.1383C>T (p.Thr461=) rs45516107 0.00545
NM_024740.2(ALG9):c.1794C>T (p.Tyr598=) rs77191760 0.00238
NM_024740.2(ALG9):c.790-11C>T rs188241987 0.00152
NM_024740.2(ALG9):c.1332C>T (p.His444=) rs139516254 0.00036
NM_024740.2(ALG9):c.1659C>T (p.Pro553=) rs2276263 0.00031
NM_024740.2(ALG9):c.1750C>T (p.Arg584Trp) rs199995104 0.00025
NM_024740.2(ALG9):c.132-18T>G rs528601164 0.00008
NM_024740.2(ALG9):c.132-14T>G rs782251612 0.00001
NM_024740.2(ALG9):c.132-15T>G rs782361758 0.00001
NM_024740.2(ALG9):c.1018+19G>A
NM_024740.2(ALG9):c.132-13del
NM_024740.2(ALG9):c.1604T>G (p.Ile535Ser) rs12575909
NM_024740.2(ALG9):c.1734-17del

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