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rs863225096

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225096(C;C)
Make rs863225096(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23419926
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs863225096
ebirs863225096
HLIrs863225096
Exacrs863225096
Varsomers863225096
Maprs863225096
PheGenIrs863225096
hapmaprs863225096
1000 genomesrs863225096
hgdprs863225096
ensemblrs863225096
gopubmedrs863225096
geneviewrs863225096
scholarrs863225096
googlers863225096
pharmgkbrs863225096
gwascentralrs863225096
openSNPrs863225096
23andMers863225096
23andMe allrs863225096
SNP Nexus

SNPshotrs863225096
SNPdbers863225096
MSV3drs863225096
GWAS Ctlgrs863225096
Max Magnitude0
ClinVar
Risk rs863225096(C;C)
Alt rs863225096(C;C)
Reference rs863225096(G;G)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7 MIR208B
CLNDBN Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23889135C>G
CLNSRC
CLNACC RCV000201442.1,