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rs397516218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516218(A;C)
Make rs397516218(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position23417185
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516218
ebirs397516218
HLIrs397516218
Exacrs397516218
Varsomers397516218
Maprs397516218
PheGenIrs397516218
hapmaprs397516218
1000 genomesrs397516218
hgdprs397516218
ensemblrs397516218
gopubmedrs397516218
geneviewrs397516218
scholarrs397516218
googlers397516218
pharmgkbrs397516218
gwascentralrs397516218
openSNPrs397516218
23andMers397516218
23andMe allrs397516218
SNP Nexus

SNPshotrs397516218
SNPdbers397516218
MSV3drs397516218
GWAS Ctlgrs397516218
Max Magnitude0
ClinVar
Risk rs397516218(C;C)
Alt rs397516218(C;C)
Reference rs397516218(A;A)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYH7 MHRT
CLNDBN not specified not provided
Reversed 1
HGVS NC_000014.8:g.23886394T>G
CLNSRC ClinVar
CLNACC RCV000035915.3, RCV000225735.1,