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rs727503271

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503271(A;A)
Make rs727503271(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429901
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503271
ebirs727503271
HLIrs727503271
Exacrs727503271
Varsomers727503271
Maprs727503271
PheGenIrs727503271
hapmaprs727503271
1000 genomesrs727503271
hgdprs727503271
ensemblrs727503271
gopubmedrs727503271
geneviewrs727503271
scholarrs727503271
googlers727503271
pharmgkbrs727503271
gwascentralrs727503271
openSNPrs727503271
23andMers727503271
23andMe allrs727503271
SNP Nexus

SNPshotrs727503271
SNPdbers727503271
MSV3drs727503271
GWAS Ctlgrs727503271
Max Magnitude0
ClinVar
Risk rs727503271(A;A)
Alt rs727503271(A;A)
Reference rs727503271(G;G)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23899110C>T
CLNSRC
CLNACC RCV000151300.1, RCV000158778.1,