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rs397516139

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516139(A;A)
Make rs397516139(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425752
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516139
ebirs397516139
HLIrs397516139
Exacrs397516139
Varsomers397516139
Maprs397516139
PheGenIrs397516139
hapmaprs397516139
1000 genomesrs397516139
hgdprs397516139
ensemblrs397516139
gopubmedrs397516139
geneviewrs397516139
scholarrs397516139
googlers397516139
pharmgkbrs397516139
gwascentralrs397516139
openSNPrs397516139
23andMers397516139
23andMe allrs397516139
SNP Nexus

SNPshotrs397516139
SNPdbers397516139
MSV3drs397516139
GWAS Ctlgrs397516139
Max Magnitude0
ClinVar
Risk rs397516139(A,C;A,C)
Alt rs397516139(A,C;A,C)
Reference rs397516139(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYH7
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23894961C>G; NC_000014.8:g.23894961C>T
CLNSRC
CLNACC RCV000158524.2, RCV000035780.2,