{{Rsnum
|rsid=892055
|Gene=RASGRP4
|Chromosome=19
|position=38422124
|Orientation=plus
|GMAF=0.4894
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=RASGRP4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 38.1 | 46.0 | 15.9
| HCB | 13.1 | 43.1 | 43.8
| JPT | 30.1 | 46.9 | 23.0
| YRI | 15.6 | 51.7 | 32.7
| ASW | 14.0 | 50.9 | 35.1
| CHB | 13.1 | 43.1 | 43.8
| CHD | 23.9 | 44.0 | 32.1
| GIH | 16.8 | 56.4 | 26.7
| LWK | 10.9 | 34.5 | 54.5
| MEX | 39.7 | 46.6 | 13.8
| MKK | 9.6 | 48.7 | 41.7
| TSI | 47.1 | 38.2 | 14.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21182207
|Trait=None
|Title=Variants in several genomic regions associated with Asperger disorder
|RiskAllele=
|Pval=0.000005
|OR=None
|ORtxt=None
}}

{{GET Evidence
|gene=RASGRP4
|aa_change=Ile18Thr
|aa_change_short=I18T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs892055
|overall_frequency_n=4143
|overall_frequency_d=9798
|overall_frequency=0.422841
|n_genomes=44
|n_genomes_annotated=0
|n_haplomes=55
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}