{{Rsnum
|rsid=4630153
|Gene=ALG6
|Chromosome=1
|position=63415881
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.219
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ALG6
}}{{omim
| id = 604566
| variant = 0002
| desc    = CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic
| rsnum   = 4630153
}}

{{GET Evidence
|gene=ALG6
|aa_change=Ser304Phe
|aa_change_short=S304F
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4630153
|overall_frequency_n=99
|overall_frequency_d=120
|overall_frequency=0.825
|n_genomes=47
|n_genomes_annotated=0
|n_haplomes=82
|n_articles=1
|n_articles_annotated=1
|qualityscore_in_silico=3
|qualitycomment_in_silico=Y
|qualityscore_in_vitro=1
|qualitycomment_in_vitro=Y
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=5
|autoscore=3
|n_web_uneval=1
}}

{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000081560.2
|CLNALLE=1
|CLNDBN=AllHighlyPenetrant
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|CLNHGVS=NC_000001.11:g.63415881C>T
|CLNORIGIN=1
|CLNSIG=2
|CLNSRC=ClinVar; Emory University
|CLNSRCID=NM_013339.3:c.911C>T; 5178
|Disease=AllHighlyPenetrant
|FwdALT=T
|FwdREF=C
|GENEINFO=ALG6:29929
|GENE_ID=29929
|GENE_NAME=ALG6
|REF=C
|RSPOS=63415881
|Reversed=0
|SAO=0
|SSR=0
|Tags=SLO;NSM;REF;ASP;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG
|VC=SNV
|VP=0x050100000a0517051e000100
|WGT=1
|dbSNPBuildID=111
|rsid=4630153
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}