{{Rsnum
|rsid=35034250
|Gene=BTD
|Chromosome=3
|position=15645027
|Orientation=plus
|GMAF=0.008724
|Gene_s=BTD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}Also known as BTD P391S.

According to http://www.arup.utah.edu/database/BTD/BTD_display.php this variant is benign. It has been observed as pathogenic only in combination with other variants.

{{GET Evidence
|gene=BTD
|aa_change=Pro391Ser
|aa_change_short=P391S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs35034250
|overall_frequency_n=183
|overall_frequency_d=10758
|overall_frequency=0.0170106
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=3
|autoscore=3
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}