List of variants in gene ALG13 reported as benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_001099922.3(ALG13):c.1435+5A>T	rs5985638	0.26139
NM_001099922.3(ALG13):c.1293A>G (p.Pro431=)	rs7063657	0.10222
NM_001099922.3(ALG13):c.1266T>C (p.Gly422=)	rs5985637	0.01375
NM_001099922.3(ALG13):c.183C>T (p.Tyr61=)	rs146925326	0.00950
NM_001099922.3(ALG13):c.2401+12C>A	rs150294098	0.00767
NM_001099922.3(ALG13):c.1152G>A (p.Ala384=)	rs145353928	0.00643
NM_001099922.3(ALG13):c.383+1029A>G	rs139631003	0.00591
NM_001099922.3(ALG13):c.2799T>A (p.Pro933=)	rs13440710	0.00508
NM_001099922.3(ALG13):c.3039A>G (p.Val1013=)	rs183032531	0.00394
NM_001099922.3(ALG13):c.2672C>T (p.Ser891Phe)	rs200066623	0.00390
NM_001099922.3(ALG13):c.2248-4A>G	rs370438099	0.00325
NM_001099922.3(ALG13):c.2898T>C (p.Tyr966=)	rs368002375	0.00247
NM_001099922.3(ALG13):c.2617G>C (p.Ala873Pro)	rs142841538	0.00166
NM_001099922.3(ALG13):c.1591T>C (p.Leu531=)	rs112837367	0.00085
NM_001099922.3(ALG13):c.3093A>G (p.Gln1031=)	rs372260338	0.00065
NM_001099922.3(ALG13):c.2248-15G>C	rs139711892	0.00040
NM_001099922.3(ALG13):c.638G>A (p.Ser213Asn)	rs374748006	0.00040
NM_001099922.3(ALG13):c.383+1033G>A	rs772039609	0.00017
NM_001099922.3(ALG13):c.1304A>G (p.Asn435Ser)	rs747478031	0.00005
NM_001099922.3(ALG13):c.360T>C (p.Gly120=)	rs747837898	0.00002
NM_001099922.3(ALG13):c.2797CCT[12] (p.Pro945del)	rs56717389
NM_001099922.3(ALG13):c.751-8_751-6del	rs765948340

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