{{Rsnum
|rsid=6582584
|Gene=ALG10B
|Chromosome=12
|position=38318340
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.03444
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=ALG10B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 1.6 | 11.3 | 87.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=6582584
|allele=G
|frequency=1
|uid=1103649417773
|type=homozygous_SNP
|hugo=AG10B_HUMAN
|ensembl gene=ENSG00000175548
|ensembl transcript=ENST00000308742
|sift=TOLERATED
|disease=Defects in ALG10B may reduce susceptibility to acquired long QT syndrome (aLQTS) (MIM:152427). It is a cardiac anomaly characterized by a paradoxical life-threatening cardiac rhythm disturbance.
}}

{{GET Evidence
|gene=ALG10B
|aa_change=Ala84Gly
|aa_change_short=A84G
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6582584
|overall_frequency_n=10376
|overall_frequency_d=10758
|overall_frequency=0.964492
|n_genomes=53
|n_genomes_annotated=0
|n_haplomes=102
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{on chip | HumanOmni1Quad}}