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

rs397516114

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516114(A;A)
Make rs397516114(A;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23427875
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516114
ebirs397516114
HLIrs397516114
Exacrs397516114
Varsomers397516114
Maprs397516114
PheGenIrs397516114
hapmaprs397516114
1000 genomesrs397516114
hgdprs397516114
ensemblrs397516114
gopubmedrs397516114
geneviewrs397516114
scholarrs397516114
googlers397516114
pharmgkbrs397516114
gwascentralrs397516114
openSNPrs397516114
23andMers397516114
23andMe allrs397516114
SNP Nexus

SNPshotrs397516114
SNPdbers397516114
MSV3drs397516114
GWAS Ctlgrs397516114
Max Magnitude0
ClinVar
Risk rs397516114(A;A)
Alt rs397516114(A;A)
Reference rs397516114(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23897084A>T
CLNSRC ClinVar
CLNACC RCV000035733.4,