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

rs397516094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516094(A;A)
Make rs397516094(A;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position23429282
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516094
ebirs397516094
HLIrs397516094
Exacrs397516094
Varsomers397516094
Maprs397516094
PheGenIrs397516094
hapmaprs397516094
1000 genomesrs397516094
hgdprs397516094
ensemblrs397516094
gopubmedrs397516094
geneviewrs397516094
scholarrs397516094
googlers397516094
pharmgkbrs397516094
gwascentralrs397516094
openSNPrs397516094
23andMers397516094
23andMe allrs397516094
SNP Nexus

SNPshotrs397516094
SNPdbers397516094
MSV3drs397516094
GWAS Ctlgrs397516094
Max Magnitude0
ClinVar
Risk rs397516094(A;A)
Alt rs397516094(A;A)
Reference rs397516094(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23898491G>A; NC_000014.8:g.23898491G>T
CLNSRC ClinVar
CLNACC RCV000223772.1, RCV000035706.4,