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

rs397516140

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516140(A;G)
Make rs397516140(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23425696
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516140
ebirs397516140
HLIrs397516140
Exacrs397516140
Varsomers397516140
Maprs397516140
PheGenIrs397516140
hapmaprs397516140
1000 genomesrs397516140
hgdprs397516140
ensemblrs397516140
gopubmedrs397516140
geneviewrs397516140
scholarrs397516140
googlers397516140
pharmgkbrs397516140
gwascentralrs397516140
openSNPrs397516140
23andMers397516140
23andMe allrs397516140
SNP Nexus

SNPshotrs397516140
SNPdbers397516140
MSV3drs397516140
GWAS Ctlgrs397516140
Max Magnitude0
ClinVar
Risk rs397516140(G;G)
Alt rs397516140(G;G)
Reference rs397516140(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23894905T>C
CLNSRC ClinVar
CLNACC RCV000035781.4,