{{Rsnum
|rsid=2317314
|Chromosome=19
|position=41555937
|Orientation=plus
|GMAF=0.4233
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CEACAM21
|Gene_s=CEACAM21
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 20.7 | 44.1 | 35.1
| HCB | 18.2 | 51.8 | 29.9
| JPT | 26.5 | 45.1 | 28.3
| YRI | 20.4 | 44.9 | 34.7
| ASW | 17.5 | 47.4 | 35.1
| CHB | 18.2 | 51.8 | 29.9
| CHD | 17.6 | 45.4 | 37.0
| GIH | 31.7 | 43.6 | 24.8
| LWK | 12.7 | 41.8 | 45.5
| MEX | 25.9 | 43.1 | 31.0
| MKK | 24.4 | 47.4 | 28.2
| TSI | 21.0 | 59.0 | 20.0
| HapMapRevision=28
}}

{{omim
|desc=DIARRHEA 3, SECRETORY SODIUM, CONGENITAL; DIAR3
|id=270420
|rsnum=2317314
}}

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

{{on chip | Affy GenomeWide 6}}