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rs199577321

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199577321(C;G)
Make rs199577321(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23433705
GeneMYH7
is asnp
is mentioned by
dbSNPrs199577321
ebirs199577321
HLIrs199577321
Exacrs199577321
Varsomers199577321
Maprs199577321
PheGenIrs199577321
hapmaprs199577321
1000 genomesrs199577321
hgdprs199577321
ensemblrs199577321
gopubmedrs199577321
geneviewrs199577321
scholarrs199577321
googlers199577321
pharmgkbrs199577321
gwascentralrs199577321
openSNPrs199577321
23andMers199577321
23andMe allrs199577321
SNP Nexus

SNPshotrs199577321
SNPdbers199577321
MSV3drs199577321
GWAS Ctlgrs199577321
Max Magnitude0
ClinVar
Risk rs199577321(G,T;G,T)
Alt rs199577321(G,T;G,T)
Reference rs199577321(C;C)
Significance Other
Disease not specified not provided Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN not specified not provided Familial hypertrophic cardiomyopathy 1
Reversed 0
HGVS NC_000014.8:g.23902914C>G; NC_000014.8:g.23902914C>T
CLNSRC
CLNACC RCV000154353.2, RCV000172568.2, RCV000156860.1, RCV000168830.1,