{{Rsnum
|rsid=644827
|Gene=SLC44A4
|Chromosome=6
|position=31870664
|Orientation=plus
|GMAF=0.3893
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC44A4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.1 | 48.7 | 21.2
| HCB | 31.4 | 47.4 | 21.2
| JPT | 42.5 | 43.4 | 14.2
| YRI | 35.4 | 47.6 | 17.0
| ASW | 45.6 | 43.9 | 10.5
| CHB | 31.4 | 47.4 | 21.2
| CHD | 37.6 | 49.5 | 12.8
| GIH | 27.7 | 53.5 | 18.8
| LWK | 51.8 | 43.6 | 4.5
| MEX | 48.3 | 43.1 | 8.6
| MKK | 39.1 | 51.3 | 9.6
| TSI | 41.2 | 47.1 | 11.8
| HapMapRevision=28
}}{{Venter SNP
|rsid=644827
|allele=C
|frequency=0.467
|uid=1103652827423
|type=homozygous_SNP
|hugo=SLC44A4
|ensembl gene=ENSG00000204385
|ensembl transcript=ENST00000375582
|sift=TOLERATED
|disease=A chromosomal aberration involving CTL4 is a cause of sialidosis, a lysosomal storage disease (MIM:256550). A rearrangement with NEU1 generates the CTL4-NEU1 transcript by fusing CTL4 to the 3'end of NEU1.
}}

{{ neighbor
| rsid = 2242665
| distance = 868
}}

{{GET Evidence
|gene=SLC44A4
|aa_change=Met326Val
|aa_change_short=M326V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs644827
|overall_frequency_n=4512
|overall_frequency_d=7518
|overall_frequency=0.60016
|n_genomes=42
|n_genomes_annotated=0
|n_haplomes=65
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}