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

rs397516196

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516196(A;A)
Make rs397516196(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23419293
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs397516196
ebirs397516196
HLIrs397516196
Exacrs397516196
Varsomers397516196
Maprs397516196
PheGenIrs397516196
hapmaprs397516196
1000 genomesrs397516196
hgdprs397516196
ensemblrs397516196
gopubmedrs397516196
geneviewrs397516196
scholarrs397516196
googlers397516196
pharmgkbrs397516196
gwascentralrs397516196
openSNPrs397516196
23andMers397516196
23andMe allrs397516196
SNP Nexus

SNPshotrs397516196
SNPdbers397516196
MSV3drs397516196
GWAS Ctlgrs397516196
Max Magnitude0
ClinVar
Risk rs397516196(A;A)
Alt rs397516196(A;A)
Reference Rs397516196(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MIR208B
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23888502C>T
CLNSRC ClinVar
CLNACC RCV000035871.3,