Have questions? Visit https://www.reddit.com/r/SNPedia

rs727503277

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503277(C;T)
Make rs727503277(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431768
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503277
ebirs727503277
HLIrs727503277
Exacrs727503277
Varsomers727503277
Maprs727503277
PheGenIrs727503277
hapmaprs727503277
1000 genomesrs727503277
hgdprs727503277
ensemblrs727503277
gopubmedrs727503277
geneviewrs727503277
scholarrs727503277
googlers727503277
pharmgkbrs727503277
gwascentralrs727503277
openSNPrs727503277
23andMers727503277
23andMe allrs727503277
SNP Nexus

SNPshotrs727503277
SNPdbers727503277
MSV3drs727503277
GWAS Ctlgrs727503277
Max Magnitude0
ClinVar
Risk rs727503277(T;T)
Alt rs727503277(T;T)
Reference rs727503277(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23900977G>A
CLNSRC
CLNACC RCV000151310.3,