{{Rsnum
|rsid=897453
|Gene=PEMT
|Chromosome=17
|position=17522317
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.2466
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PEMT
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 23.2 | 48.2 | 28.6
| HCB | 0.0 | 6.7 | 93.3
| JPT | 3.5 | 31.9 | 64.6
| YRI | 0.0 | 7.5 | 92.5
| ASW | 1.8 | 24.6 | 73.7
| CHB | 0.0 | 6.7 | 93.3
| CHD | 0.0 | 15.0 | 85.0
| GIH | 5.1 | 35.4 | 59.6
| LWK | 0.0 | 9.2 | 90.8
| MEX | 12.3 | 42.1 | 45.6
| MKK | 2.0 | 17.0 | 81.0
| TSI | 16.7 | 46.1 | 37.3
| HapMapRevision=28
}}

{{Venter SNP
|rsid=897453
|allele=G
|frequency=
|uid=1103645292897
|type=homozygous_SNP
|hugo=PEMT
|ensembl gene=ENSG00000133027
|ensembl transcript=ENST00000343219
|sift=TOLERATED
|disease=Deletion of PEMT may be related to liver cancer.
}}

{{GET Evidence
|gene=PEMT
|aa_change=Val95Ile
|aa_change_short=V95I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs897453
|overall_frequency_n=3643
|overall_frequency_d=10758
|overall_frequency=0.338632
|n_genomes=21
|n_genomes_annotated=0
|n_haplomes=27
|n_articles=0
|n_articles_annotated=0
|nblosum100=-4
|autoscore=0
|webscore=N
}}

{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}