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rs730880857

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880857(C;C)
Make rs730880857(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23430925
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880857
ebirs730880857
HLIrs730880857
Exacrs730880857
Varsomers730880857
Maprs730880857
PheGenIrs730880857
hapmaprs730880857
1000 genomesrs730880857
hgdprs730880857
ensemblrs730880857
gopubmedrs730880857
geneviewrs730880857
scholarrs730880857
googlers730880857
pharmgkbrs730880857
gwascentralrs730880857
openSNPrs730880857
23andMers730880857
23andMe allrs730880857
SNP Nexus

SNPshotrs730880857
SNPdbers730880857
MSV3drs730880857
GWAS Ctlgrs730880857
Max Magnitude0
ClinVar
Risk rs730880857(C;C)
Alt rs730880857(C;C)
Reference rs730880857(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23900134A>G
CLNSRC
CLNACC RCV000158770.2,