{{Rsnum
|rsid=6591182
|Gene=EHBP1L1
|Chromosome=11
|position=65582285
|Orientation=plus
|GMAF=0.4316
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=EHBP1L1
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 23.0 | 47.8 | 29.2
| HCB | 30.7 | 43.1 | 26.3
| JPT | 17.7 | 53.1 | 29.2
| YRI | 10.2 | 42.2 | 47.6
| ASW | 12.3 | 31.6 | 56.1
| CHB | 30.7 | 43.1 | 26.3
| CHD | 12.8 | 51.4 | 35.8
| GIH | 17.0 | 62.0 | 21.0
| LWK | 10.9 | 50.9 | 38.2
| MEX | 12.1 | 43.1 | 44.8
| MKK | 18.7 | 49.7 | 31.6
| TSI | 22.5 | 52.0 | 25.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20708005
|Trait=None
|Title=Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease
|RiskAllele=A
|Pval=9E-7
|OR=0.54
|ORtxt=[NR] unit increase
|OA=1
}}

{{GET Evidence
|gene=EHBP1L1
|aa_change=Val538Gly
|aa_change_short=V538G
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6591182
|overall_frequency_n=4000
|overall_frequency_d=9608
|overall_frequency=0.41632
|n_genomes=42
|n_genomes_annotated=0
|n_haplomes=53
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.992
|nblosum100=8
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}