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rs727503274

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503274(A;G)
Make rs727503274(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23430948
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503274
ebirs727503274
HLIrs727503274
Exacrs727503274
Varsomers727503274
Maprs727503274
PheGenIrs727503274
hapmaprs727503274
1000 genomesrs727503274
hgdprs727503274
ensemblrs727503274
gopubmedrs727503274
geneviewrs727503274
scholarrs727503274
googlers727503274
pharmgkbrs727503274
gwascentralrs727503274
openSNPrs727503274
23andMers727503274
23andMe allrs727503274
SNP Nexus

SNPshotrs727503274
SNPdbers727503274
MSV3drs727503274
GWAS Ctlgrs727503274
Max Magnitude0
ClinVar
Risk rs727503274(G;G)
Alt rs727503274(G;G)
Reference rs727503274(A;A)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYH7
CLNDBN not specified not provided
Reversed 1
HGVS NC_000014.8:g.23900157T>C
CLNSRC
CLNACC RCV000151306.2, RCV000158769.2,