{{Rsnum
|rsid = 28932774
|Gene = MYL2
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=12
|position=110919145
|Gene_s=MYL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
| Status = Merged
| Merged = 104894370
}}[[Familial hypertrophic cardiomyopathy]]

see also OMIM [http://omim.org/entry/160781#0005 160781.0005]

Note: this SNP, [[rs28932774]], appears to tag the same polymorphism as [[rs104894370]]


{{omim
| id = 160781
| variant = 0005
| desc    = CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
| rsnum   = 28932774
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}