{{Rsnum
|rsid=227368
|Gene=MANBA
|Chromosome=4
|position=102690688
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=T
|GMAF=0.3972
|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 | 17.7 | 58.4 | 23.9
| HCB | 26.3 | 50.4 | 23.4
| JPT | 33.6 | 46.0 | 20.4
| YRI | 1.4 | 20.4 | 78.2
| ASW | 0.0 | 28.1 | 71.9
| CHB | 26.3 | 50.4 | 23.4
| CHD | 27.8 | 47.2 | 25.0
| GIH | 18.8 | 55.4 | 25.7
| LWK | 1.8 | 22.7 | 75.5
| MEX | 5.2 | 44.8 | 50.0
| MKK | 0.6 | 27.6 | 71.8
| TSI | 20.6 | 54.9 | 24.5
| HapMapRevision=28
}}

{{Venter SNP
|rsid=227368
|allele=G
|frequency=0.45
|uid=1103654502060
|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=Val253Ile
|aa_change_short=V253I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs227368
|overall_frequency_n=4125
|overall_frequency_d=10758
|overall_frequency=0.383436
|n_genomes=27
|n_genomes_annotated=0
|n_haplomes=34
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.003
|genetests_testable=Y
|nblosum100=-4
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}