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rs730880865

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880865(G;G)
Make rs730880865(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429843
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880865
ebirs730880865
HLIrs730880865
Exacrs730880865
Varsomers730880865
Maprs730880865
PheGenIrs730880865
hapmaprs730880865
1000 genomesrs730880865
hgdprs730880865
ensemblrs730880865
gopubmedrs730880865
geneviewrs730880865
scholarrs730880865
googlers730880865
pharmgkbrs730880865
gwascentralrs730880865
openSNPrs730880865
23andMers730880865
23andMe allrs730880865
SNP Nexus

SNPshotrs730880865
SNPdbers730880865
MSV3drs730880865
GWAS Ctlgrs730880865
Max Magnitude0
ClinVar
Risk rs730880865(G;G)
Alt rs730880865(G;G)
Reference rs730880865(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23899052A>C
CLNSRC
CLNACC RCV000158783.1,