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rs727503268

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503268(A;A)
Make rs727503268(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429320
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503268
ebirs727503268
HLIrs727503268
Exacrs727503268
Varsomers727503268
Maprs727503268
PheGenIrs727503268
hapmaprs727503268
1000 genomesrs727503268
hgdprs727503268
ensemblrs727503268
gopubmedrs727503268
geneviewrs727503268
scholarrs727503268
googlers727503268
pharmgkbrs727503268
gwascentralrs727503268
openSNPrs727503268
23andMers727503268
23andMe allrs727503268
SNP Nexus

SNPshotrs727503268
SNPdbers727503268
MSV3drs727503268
GWAS Ctlgrs727503268
Max Magnitude0
ClinVar
Risk rs727503268(A;A)
Alt rs727503268(A;A)
Reference rs727503268(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23898529C>T
CLNSRC
CLNACC RCV000151295.2,