{{Rsnum
|rsid=2278206
|Gene=INPP4A
|Chromosome=2
|position=98555781
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.275
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=INPP4A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 5.3 | 35.4 | 59.3
| HCB | 8.8 | 37.2 | 54.0
| JPT | 8.0 | 43.4 | 48.7
| YRI | 3.4 | 25.9 | 70.7
| ASW | 8.8 | 36.8 | 54.4
| CHB | 8.8 | 37.2 | 54.0
| CHD | 9.2 | 37.6 | 53.2
| GIH | 8.9 | 45.5 | 45.5
| LWK | 12.7 | 42.7 | 44.5
| MEX | 1.7 | 50.0 | 48.3
| MKK | 9.6 | 39.7 | 50.6
| TSI | 10.8 | 40.2 | 49.0
| HapMapRevision=28
}}A study of ~170 families led to a slight association between [[rs2278206]] and atopic [[asthma]]. The risk genotype - in dbSNP orientation, not as published - is [[rs2278206]](T;T). Conversely, the [[rs2278206]](C;C) genotype was rarely (odds ratio 0.13) seen in patients with atopic asthma.{{PMID|18187694}}

{{GET Evidence
|gene=INPP4A
|aa_change=Thr604Ala
|aa_change_short=T604A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2278206
|overall_frequency_n=804
|overall_frequency_d=3234
|overall_frequency=0.248609
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=0
|webscore=N
}}

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