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rs28932774

From SNPedia

Merged intors104894370
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 3 Familial Hypertrophic Cardiomyopathy
(C;T) 3 Familial Hypertrophic Cardiomyopathy
(T;T) 0
ReferenceGRCh38 38.1/141
Chromosome12
Position110919145
GeneMYL2
is asnp
is mentioned by
dbSNPrs28932774
ebirs28932774
HLIrs28932774
Exacrs28932774
Varsomers28932774
Maprs28932774
PheGenIrs28932774
hapmaprs28932774
1000 genomesrs28932774
hgdprs28932774
ensemblrs28932774
gopubmedrs28932774
geneviewrs28932774
scholarrs28932774
googlers28932774
pharmgkbrs28932774
gwascentralrs28932774
openSNPrs28932774
23andMers28932774
23andMe allrs28932774
SNP Nexus

SNPshotrs28932774
SNPdbers28932774
MSV3drs28932774
GWAS Ctlgrs28932774
StatusMerged into rs104894370
Max Magnitude3
Familial hypertrophic cardiomyopathy

see also OMIM 160781.0005

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


OMIM160781
DescCARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
Variant0005
Relatedalso