{{Rsnum
|rsid=1836915
|Gene=MME
|Chromosome=3
|position=155091313
|Orientation=plus
|GMAF=0.1061
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MME
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 27.4 | 71.7
| HCB | 0.0 | 18.2 | 81.8
| JPT | 0.9 | 14.2 | 85.0
| YRI | 0.0 | 20.6 | 79.4
| ASW | 0.0 | 24.6 | 75.4
| CHB | 0.0 | 18.2 | 81.8
| CHD | 0.0 | 19.3 | 80.7
| GIH | 0.0 | 18.8 | 81.2
| LWK | 1.8 | 7.3 | 90.9
| MEX | 0.0 | 6.9 | 93.1
| MKK | 4.5 | 11.0 | 84.5
| TSI | 1.0 | 27.5 | 71.6
| HapMapRevision=28
}}[[rs1836915]] is a SNP in the membrane metalloendopeptidase [[MME]] gene, which is also known as CD10, CALLA or neprilysin.

[[rs1836915]] showed the strongest association among several [[MME]] SNPs to [[Alzheimer's disease]] in a study of 298 Caucasian patients.{{PMID|17928142}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}