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rs727504385

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504385(A;G)
Make rs727504385(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23415210
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs727504385
ebirs727504385
HLIrs727504385
Exacrs727504385
Varsomers727504385
Maprs727504385
PheGenIrs727504385
hapmaprs727504385
1000 genomesrs727504385
hgdprs727504385
ensemblrs727504385
gopubmedrs727504385
geneviewrs727504385
scholarrs727504385
googlers727504385
pharmgkbrs727504385
gwascentralrs727504385
openSNPrs727504385
23andMers727504385
23andMe allrs727504385
SNP Nexus

SNPshotrs727504385
SNPdbers727504385
MSV3drs727504385
GWAS Ctlgrs727504385
Max Magnitude0
ClinVar
Risk rs727504385(G;G)
Alt rs727504385(G;G)
Reference Rs727504385(A;A)
Significance Probable-Pathogenic
Disease not specified Hypertrophic cardiomyopathy
Variation info
Gene MYH7 MHRT
CLNDBN not specified Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23884419T>C
CLNSRC
CLNACC RCV000154544.2, RCV000168424.2,