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rs727504240

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504240(C;T)
Make rs727504240(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23426046
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504240
ebirs727504240
HLIrs727504240
Exacrs727504240
Varsomers727504240
Maprs727504240
PheGenIrs727504240
hapmaprs727504240
1000 genomesrs727504240
hgdprs727504240
ensemblrs727504240
gopubmedrs727504240
geneviewrs727504240
scholarrs727504240
googlers727504240
pharmgkbrs727504240
gwascentralrs727504240
openSNPrs727504240
23andMers727504240
23andMe allrs727504240
SNP Nexus

SNPshotrs727504240
SNPdbers727504240
MSV3drs727504240
GWAS Ctlgrs727504240
Max Magnitude0
ClinVar
Risk rs727504240(T;T)
Alt rs727504240(T;T)
Reference rs727504240(C;C)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23895255G>A
CLNSRC
CLNACC RCV000154206.2, RCV000158506.2,