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rs397516233

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516233(G;T)
Make rs397516233(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23415832
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516233
ebirs397516233
HLIrs397516233
Exacrs397516233
Varsomers397516233
Maprs397516233
PheGenIrs397516233
hapmaprs397516233
1000 genomesrs397516233
hgdprs397516233
ensemblrs397516233
gopubmedrs397516233
geneviewrs397516233
scholarrs397516233
googlers397516233
pharmgkbrs397516233
gwascentralrs397516233
openSNPrs397516233
23andMers397516233
23andMe allrs397516233
SNP Nexus

SNPshotrs397516233
SNPdbers397516233
MSV3drs397516233
GWAS Ctlgrs397516233
Max Magnitude0
ClinVar
Risk rs397516233(A,T;A,T)
Alt rs397516233(A,T;A,T)
Reference rs397516233(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23885041C>A
CLNSRC ClinVar
CLNACC RCV000035941.3,