ClinVar Miner

List of variants in gene ALG9 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_024740.2(ALG9):c.*2473A>T rs2554994 0.69652
NM_024740.2(ALG9):c.*2474A>T rs376483443 0.04275
NM_024740.2(ALG9):c.*1607C>T rs117488631 0.00826
NM_024740.2(ALG9):c.*1680G>T rs563719515 0.00575
NM_024740.2(ALG9):c.*2010_*2011del rs534577430 0.00567
NM_024740.2(ALG9):c.*1681dup rs541176886 0.00510
NM_024740.2(ALG9):c.*1624A>C rs117091304 0.00485
NM_024740.2(ALG9):c.*2230A>C rs116530919 0.00264
NM_024740.2(ALG9):c.*3471A>G rs186742619 0.00264
NM_024740.2(ALG9):c.*1722C>T rs186477879 0.00192
NM_024740.2(ALG9):c.*3423T>C rs78243190 0.00176
NM_024740.2(ALG9):c.*3519C>A rs569799426 0.00145
NM_024740.2(ALG9):c.*1420C>G rs143933458 0.00121
NM_024740.2(ALG9):c.*3757T>C rs530143933 0.00093
NM_024740.2(ALG9):c.*3175G>A rs146182772 0.00078
NM_024740.2(ALG9):c.*314G>A rs781928817 0.00077
NM_024740.2(ALG9):c.*823A>G rs528387467 0.00058
NM_024740.2(ALG9):c.*3358dup rs782323400 0.00056
NM_024740.2(ALG9):c.*1977A>G rs181231005 0.00043
NM_024740.2(ALG9):c.*2114C>T rs45452093 0.00034
NM_024740.2(ALG9):c.*2287A>G rs185264895 0.00034
NM_024740.2(ALG9):c.*2414T>G rs189536081 0.00034
NM_024740.2(ALG9):c.*1536T>C rs782678326 0.00032
NM_024740.2(ALG9):c.*2472T>A rs886047667 0.00023
NM_024740.2(ALG9):c.*2457G>T rs201995459 0.00022
NM_024740.2(ALG9):c.*3213G>A rs939244636 0.00021
NM_024740.2(ALG9):c.*1832A>C rs772136205 0.00017
NM_024740.2(ALG9):c.*906C>A rs147670080 0.00010
NM_024740.2(ALG9):c.-58A>G rs782440068 0.00010
NM_024740.2(ALG9):c.*2233A>G rs886047674 0.00009
NM_024740.2(ALG9):c.*229A>G rs781789551 0.00009
NM_024740.2(ALG9):c.*2907A>T rs782731018 0.00008
NM_024740.2(ALG9):c.*1307C>T rs782298169 0.00006
NM_024740.2(ALG9):c.*305C>T rs782183793 0.00006
NM_024740.2(ALG9):c.*523T>C rs536072357 0.00006
NM_024740.2(ALG9):c.*4141G>C rs541035545 0.00004
NM_024740.2(ALG9):c.*763T>C rs886047680 0.00004
NM_024740.2(ALG9):c.*1687A>T rs367569393 0.00003
NM_024740.2(ALG9):c.*2339T>G rs886047673 0.00003
NM_024740.2(ALG9):c.*306G>A rs886047683 0.00003
NM_024740.2(ALG9):c.*773A>G rs886047679 0.00003
NM_024740.2(ALG9):c.1660C>T (p.Arg554Trp) rs782084496 0.00003
NM_024740.2(ALG9):c.*1311A>G rs912924184 0.00002
NM_024740.2(ALG9):c.*2342G>A rs532591210 0.00001
NM_024740.2(ALG9):c.*3079C>T rs886047660 0.00001
NM_024740.2(ALG9):c.*3125A>T rs547384257 0.00001
NM_024740.2(ALG9):c.*3212C>T rs528920657 0.00001
NM_024740.2(ALG9):c.*365A>G rs886047682 0.00001
NM_024740.2(ALG9):c.*726C>G rs1414677485 0.00001
NM_024740.2(ALG9):c.*77G>A rs984910253 0.00001
NM_024740.2(ALG9):c.*788A>G rs559698025 0.00001
NM_024740.2(ALG9):c.*1211AGTT[1] rs782618635
NM_024740.2(ALG9):c.*1297A>G rs577487864
NM_024740.2(ALG9):c.*1679del rs150703313
NM_024740.2(ALG9):c.*1679dup rs150703313
NM_024740.2(ALG9):c.*1766A>G rs886047676
NM_024740.2(ALG9):c.*243G>A rs886047684
NM_024740.2(ALG9):c.*2442del rs886047672
NM_024740.2(ALG9):c.*2443T>A rs146821834
NM_024740.2(ALG9):c.*2444_*2449del rs886047670
NM_024740.2(ALG9):c.*2444del rs886047671
NM_024740.2(ALG9):c.*2451_*2457del rs886047668
NM_024740.2(ALG9):c.*2456del rs886047669
NM_024740.2(ALG9):c.*2473_*2474insT rs886047666
NM_024740.2(ALG9):c.*2474_*2475insT rs886047665
NM_024740.2(ALG9):c.*2479del rs376955296
NM_024740.2(ALG9):c.*2480_*2481del rs886047663
NM_024740.2(ALG9):c.*2480del rs886047664
NM_024740.2(ALG9):c.*2592T>C rs886047661
NM_024740.2(ALG9):c.*2597G>C rs1591752692
NM_024740.2(ALG9):c.*2648G>A rs1946165207
NM_024740.2(ALG9):c.*3437_*3440del rs371625196
NM_024740.2(ALG9):c.*3798A>G rs1946041440
NM_024740.2(ALG9):c.*3954del rs573760463
NM_024740.2(ALG9):c.*532C>T rs886047681

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