{{Rsnum
|rsid=2866413
|Gene=MANBA
|Chromosome=4
|position=102635920
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.449
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MANBA
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 25.7 | 56.6 | 17.7
| HCB | 19.0 | 54.7 | 26.3
| JPT | 24.8 | 46.9 | 28.3
| YRI | 42.9 | 46.9 | 10.2
| ASW | 45.6 | 42.1 | 12.3
| CHB | 19.0 | 54.7 | 26.3
| CHD | 20.4 | 50.9 | 28.7
| GIH | 20.8 | 47.5 | 31.7
| LWK | 33.6 | 53.6 | 12.7
| MEX | 48.3 | 46.6 | 5.2
| MKK | 39.1 | 44.2 | 16.7
| TSI | 20.6 | 56.9 | 22.5
| HapMapRevision=28
}}{{Venter SNP
|rsid=2866413
|allele=A
|frequency=0.408
|uid=1103654501958
|type=heterozygous_SNP
|hugo=MANBA
|ensembl gene=ENSG00000109323
|ensembl transcript=ENST00000226578
|sift=TOLERATED
|disease=Defects in MANBA are the cause of a mild disorder that affects peripheral and central nervous system myelin.
}}

{{GET Evidence
|gene=MANBA
|aa_change=Thr701Met
|aa_change_short=T701M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2866413
|overall_frequency_n=5934
|overall_frequency_d=10758
|overall_frequency=0.551589
|n_genomes=45
|n_genomes_annotated=0
|n_haplomes=61
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=2
|autoscore=2
|n_web_uneval=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}