{{Rsnum
|rsid=17114699
|Gene=ANG
|Chromosome=14
|position=20690751
|Orientation=plus
|GMAF=0.2071
|Gene_s=ANG,RNASE4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 80.5 | 18.6 | 0.9
| HCB | 67.9 | 27.0 | 5.1
| JPT | 67.0 | 31.2 | 1.8
| YRI | 18.4 | 51.7 | 29.9
| ASW | 28.6 | 55.4 | 16.1
| CHB | 67.9 | 27.0 | 5.1
| CHD | 72.5 | 23.9 | 3.7
| GIH | 77.0 | 22.0 | 1.0
| LWK | 30.9 | 50.0 | 19.1
| MEX | 69.0 | 31.0 | 0.0
| MKK | 49.4 | 42.3 | 8.3
| TSI | 80.4 | 19.6 | 0.0
| HapMapRevision=28
}}This SNP is located within an intron of the ANG gene which produces the Angiogenin protein. 

The T allele is associated with risk of [[amyotrophic lateral sclerosis]] ([[ALS]]) in Irish and Swedish populations, but not in Polish populations [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0015402]

{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}