{{Rsnum
|rsid=2820312
|Gene=LMOD1
|Chromosome=1
|position=201900129
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.241
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=LMOD1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 15.0 | 41.6 | 43.4
| HCB | 3.6 | 18.2 | 78.1
| JPT | 0.0 | 14.2 | 85.8
| YRI | 2.1 | 37.7 | 60.3
| ASW | 8.8 | 42.1 | 49.1
| CHB | 3.6 | 18.2 | 78.1
| CHD | 0.0 | 22.0 | 78.0
| GIH | 10.9 | 43.6 | 45.5
| LWK | 3.6 | 46.4 | 50.0
| MEX | 3.4 | 31.0 | 65.5
| MKK | 5.1 | 41.7 | 53.2
| TSI | 10.8 | 39.2 | 50.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=2820312
|allele=A
|frequency=0.292
|uid=1103675311566
|type=heterozygous_SNP
|hugo=LMOD1
|ensembl gene=ENSG00000163431
|ensembl transcript=ENST00000367288
|sift=TOLERATED
|disease=Recognized by patients with autoimmune thyroid disease.
}}

{{GET Evidence
|gene=LMOD1
|aa_change=Thr295Met
|aa_change_short=T295M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2820312
|overall_frequency_n=2792
|overall_frequency_d=10082
|overall_frequency=0.276929
|n_genomes=21
|n_genomes_annotated=0
|n_haplomes=24
|n_articles=0
|n_articles_annotated=0
|nblosum100=2
|autoscore=0
|webscore=N
}}

{{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}}