{{Rsnum
|rsid=2071152
|Gene=TRAPPC10
|Chromosome=21
|position=44083240
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.3186
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TRAPPC10
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 28.6 | 70.5
| HCB | 6.6 | 35.8 | 57.7
| JPT | 11.5 | 37.2 | 51.3
| YRI | 55.1 | 36.1 | 8.8
| ASW | 29.8 | 36.8 | 33.3
| CHB | 6.6 | 35.8 | 57.7
| CHD | 10.1 | 42.2 | 47.7
| GIH | 19.8 | 49.5 | 30.7
| LWK | 40.0 | 50.0 | 10.0
| MEX | 12.1 | 37.9 | 50.0
| MKK | 22.4 | 53.2 | 24.4
| TSI | 2.9 | 31.4 | 65.7
| HapMapRevision=28
}}

{{Venter SNP
|rsid=2071152
|allele=A
|frequency=0
|uid=1103643131080
|type=heterozygous_SNP
|hugo=TMEM1
|ensembl gene=ENSG00000160218
|ensembl transcript=ENST00000291574
|sift=TOLERATED
|disease=Candidate for autoimmune polyglandular disease type 1 (APECED).
}}

{{GET Evidence
|gene=TRAPPC10
|aa_change=Val726Met
|aa_change_short=V726M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2071152
|overall_frequency_n=3379
|overall_frequency_d=10758
|overall_frequency=0.314092
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=43
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_reviewed=Y
|nblosum100=0
|autoscore=1
|webscore=N
}}

{{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}}