List of variants in gene ALG9 studied for Congenital disorder of glycosylation

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_024740.2(ALG9):c.2010_2011del	rs534577430	0.00567
NM_024740.2(ALG9):c.*1681dup	rs541176886	0.00510
NM_024740.2(ALG9):c.*3358dup	rs782323400	0.00056
NM_024740.2(ALG9):c.*1307C>T	rs782298169	0.00006
NM_024740.2(ALG9):c.1660C>T (p.Arg554Trp)	rs782084496	0.00003
NM_024740.2(ALG9):c.*1211AGTT[1]	rs782618635
NM_024740.2(ALG9):c.*1679del	rs150703313
NM_024740.2(ALG9):c.*1679dup	rs150703313
NM_024740.2(ALG9):c.*2442del	rs886047672
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.2496_2500del	rs3833761
NM_024740.2(ALG9):c.3437_3440del	rs371625196
NM_024740.2(ALG9):c.*3954del	rs573760463

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