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rs28933099

From SNPedia

Merged intors104894369
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 3 Familial Hypertrophic Cardiomyopathy
(A;G) 3 Familial Hypertrophic Cardiomyopathy
(G;G) 0
ReferenceGRCh38 38.1/141
Chromosome12
Position110914287
GeneMYL2
is asnp
is mentioned by
dbSNPrs28933099
ebirs28933099
HLIrs28933099
Exacrs28933099
Varsomers28933099
Maprs28933099
PheGenIrs28933099
hapmaprs28933099
1000 genomesrs28933099
hgdprs28933099
ensemblrs28933099
gopubmedrs28933099
geneviewrs28933099
scholarrs28933099
googlers28933099
pharmgkbrs28933099
gwascentralrs28933099
openSNPrs28933099
23andMers28933099
23andMe allrs28933099
SNP Nexus

SNPshotrs28933099
SNPdbers28933099
MSV3drs28933099
GWAS Ctlgrs28933099
StatusMerged into rs104894369
Max Magnitude3
Familial hypertrophic cardiomyopathy

see also OMIM 160781.0004

Note: this SNP, rs28933099, appears to tag the same polymorphism as rs104894369

OMIM160781
DescCARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
Variant0004
Relatedalso