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rs727504409

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504409(C;G)
Make rs727504409(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23430997
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504409
ebirs727504409
HLIrs727504409
Exacrs727504409
Varsomers727504409
Maprs727504409
PheGenIrs727504409
hapmaprs727504409
1000 genomesrs727504409
hgdprs727504409
ensemblrs727504409
gopubmedrs727504409
geneviewrs727504409
scholarrs727504409
googlers727504409
pharmgkbrs727504409
gwascentralrs727504409
openSNPrs727504409
23andMers727504409
23andMe allrs727504409
SNP Nexus

SNPshotrs727504409
SNPdbers727504409
MSV3drs727504409
GWAS Ctlgrs727504409
Max Magnitude0
ClinVar
Risk rs727504409(G;G)
Alt rs727504409(G;G)
Reference rs727504409(C;C)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23900206G>C
CLNSRC
CLNACC RCV000154595.2,