{{Rsnum
|rsid=7258249
|Chromosome=19
|position=8206837
|Orientation=plus
|GMAF=0.2622
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 24.8 | 52.2 | 23.0
| HCB | 0.7 | 9.5 | 89.8
| JPT | 0.0 | 9.7 | 90.3
| YRI | 2.7 | 20.4 | 76.9
| ASW | 1.8 | 28.1 | 70.2
| CHB | 0.7 | 9.5 | 89.8
| CHD | 0.0 | 10.1 | 89.9
| GIH | 8.9 | 40.6 | 50.5
| LWK | 1.8 | 30.0 | 68.2
| MEX | 8.6 | 34.5 | 56.9
| MKK | 7.1 | 41.7 | 51.3
| TSI | 23.5 | 51.0 | 25.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19798445
|Trait=Sphingolipid Concentrations
|Title=Genetic determinants of circulating sphingolipid concentrations in European populations
|RiskAllele=G
|Pval=2E-27
|OR=0
|ORtxt=[0.0007-0.001] mol % increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=22359512
|Trait=None
|Title=Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
|RiskAllele=
|Pval=1E-34
|OR=0
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7258249
|overall_frequency_n=28
|overall_frequency_d=128
|overall_frequency=0.21875
|n_genomes=20
|n_genomes_annotated=0
|n_haplomes=25
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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