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rs727504342

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504342(A;A)
Make rs727504342(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23422189
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504342
ebirs727504342
HLIrs727504342
Exacrs727504342
Varsomers727504342
Maprs727504342
PheGenIrs727504342
hapmaprs727504342
1000 genomesrs727504342
hgdprs727504342
ensemblrs727504342
gopubmedrs727504342
geneviewrs727504342
scholarrs727504342
googlers727504342
pharmgkbrs727504342
gwascentralrs727504342
openSNPrs727504342
23andMers727504342
23andMe allrs727504342
SNP Nexus

SNPshotrs727504342
SNPdbers727504342
MSV3drs727504342
GWAS Ctlgrs727504342
Max Magnitude0
ClinVar
Risk rs727504342(A;A)
Alt rs727504342(A;A)
Reference rs727504342(G;G)
Significance Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN not specified Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23891398C>T
CLNSRC Centenary Institute
CLNACC RCV000154461.2, RCV000172886.1,