{{Rsnum
|rsid=1363364
|Gene=LOC400685
|Chromosome=19
|position=34817436
|Orientation=plus
|GMAF=0.4702
|Gene_s=PEX11B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 20.3 | 56.2 | 23.4
| HCB | 24.4 | 51.1 | 24.4
| JPT | 37.2 | 46.5 | 16.3
| YRI | 3.2 | 39.7 | 57.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 24.4 | 51.1 | 24.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{omim
|desc=DIARRHEA 3, SECRETORY SODIUM, CONGENITAL; DIAR3
|id=270420
|rsnum=1363364
}}

{{PMID Auto
|PMID=19185281
|Title=Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}