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rs77613865

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs77613865(G;G)
Make rs77613865(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position3149142
GeneMYOM1
is asnp
is mentioned by
dbSNPrs77613865
ebirs77613865
HLIrs77613865
Exacrs77613865
Varsomers77613865
Maprs77613865
PheGenIrs77613865
hapmaprs77613865
1000 genomesrs77613865
hgdprs77613865
ensemblrs77613865
gopubmedrs77613865
geneviewrs77613865
scholarrs77613865
googlers77613865
pharmgkbrs77613865
gwascentralrs77613865
openSNPrs77613865
23andMers77613865
23andMe allrs77613865
SNP Nexus

SNPshotrs77613865
SNPdbers77613865
MSV3drs77613865
GWAS Ctlgrs77613865
Max Magnitude0
ClinVar
Risk rs77613865(G;G)
Alt rs77613865(G;G)
Reference rs77613865(T;T)
Significance Other
Disease Hypertrophic cardiomyopathy not specified
Variation info
Gene MYOM1
CLNDBN Hypertrophic cardiomyopathy not specified
Reversed 0
HGVS NC_000018.9:g.3149140T>G
CLNSRC
CLNACC RCV000157649.2, RCV000217695.1,