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rs727503240

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503240(A;A)
Make rs727503240(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23413859
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs727503240
ebirs727503240
HLIrs727503240
Exacrs727503240
Varsomers727503240
Maprs727503240
PheGenIrs727503240
hapmaprs727503240
1000 genomesrs727503240
hgdprs727503240
ensemblrs727503240
gopubmedrs727503240
geneviewrs727503240
scholarrs727503240
googlers727503240
pharmgkbrs727503240
gwascentralrs727503240
openSNPrs727503240
23andMers727503240
23andMe allrs727503240
SNP Nexus

SNPshotrs727503240
SNPdbers727503240
MSV3drs727503240
GWAS Ctlgrs727503240
Max Magnitude0
ClinVar
Risk rs727503240(A;A)
Alt rs727503240(A;A)
Reference rs727503240(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYH7 MHRT
CLNDBN not specified not provided
Reversed 1
HGVS NC_000014.8:g.23883068C>T
CLNSRC
CLNACC RCV000151233.1, RCV000158713.2,