{{Rsnum
|rsid=2288904
|Gene=SLC44A2
|Chromosome=19
|position=10631494
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.213
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC44A2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 59.6 | 35.8 | 4.6
| HCB | 40.4 | 49.3 | 10.3
| JPT | 42.0 | 46.4 | 11.6
| YRI | 97.2 | 2.8 | 0.0
| ASW | 82.5 | 17.5 | 0.0
| CHB | 40.4 | 49.3 | 10.3
| CHD | 43.5 | 43.5 | 13.0
| GIH | 46.5 | 46.5 | 6.9
| LWK | 90.7 | 9.3 | 0.0
| MEX | 69.0 | 29.3 | 1.7
| MKK | 77.9 | 21.4 | 0.6
| TSI | 51.5 | 42.6 | 5.9
| HapMapRevision=28
}}
[http://blog.23andme.com/2010/02/08/snpwatch-genetic-variant-involved-in-dangerous-blood-transfusion-reaction-identified/ 23andMe blog] relevant for [[blood]] transfusion compatibility.

{{Venter SNP
|rsid=2288904
|allele=G
|frequency=0.767
|uid=1103691089575
|type=homozygous_SNP
|hugo=SLC44A2
|ensembl gene=ENSG00000129353
|ensembl transcript=ENST00000335757
|sift=TOLERATED
|disease=Possible antigen for autoimmune hearing loss.
}}

{{omim
|desc=SOLUTE CARRIER FAMILY 44, MEMBER 2; SLC44A2
|id=606106
|rsnum=2288904
}}

{{GET Evidence
|gene=SLC44A2
|aa_change=Gln154Arg
|aa_change_short=Q154R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2288904
|overall_frequency_n=8992
|overall_frequency_d=10758
|overall_frequency=0.835843
|n_genomes=51
|n_genomes_annotated=0
|n_haplomes=87
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=24236643
|Title=HNA-3 gene frequencies in Brazilians and a new polymerase chain reaction-restriction fragment length polymorphism method for HNA-3a/3b genotyping
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}