{{Rsnum
|rsid=8176785
|Gene=NELL1
|Chromosome=11
|position=20783740
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.3136
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NELL1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 45.1 | 47.8 | 7.1
| HCB | 64.2 | 33.6 | 2.2
| JPT | 71.7 | 26.5 | 1.8
| YRI | 1.4 | 36.8 | 61.8
| ASW | 5.4 | 48.2 | 46.4
| CHB | 64.2 | 33.6 | 2.2
| CHD | 72.5 | 24.8 | 2.8
| GIH | 60.0 | 34.0 | 6.0
| LWK | 6.4 | 40.9 | 52.7
| MEX | 74.1 | 24.1 | 1.7
| MKK | 14.1 | 52.6 | 33.3
| TSI | 67.6 | 26.5 | 5.9
| HapMapRevision=28
}}

{{Venter SNP
|rsid=8176785
|allele=A
|frequency=0.267
|uid=1103649626724
|type=heterozygous_SNP
|hugo=NELL1
|ensembl gene=ENSG00000165973
|ensembl transcript=ENST00000298925
|sift=TOLERATED
|disease=Expressed in craniofacial anomalies.
}}

{{PMID Auto
|PMID=17684544
|Title=Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|OA=1
}}

{{GET Evidence
|gene=NELL1
|aa_change=Arg82Gln
|aa_change_short=R82Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs8176785
|overall_frequency_n=6470
|overall_frequency_d=10758
|overall_frequency=0.601413
|n_genomes=38
|n_genomes_annotated=0
|n_haplomes=59
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=22495925
|Title=Genetic polymorphisms inside and outside the MHC improve prediction of AS radiographic severity in addition to clinical variables.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}