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rs730880842

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880842(A;C)
Make rs730880842(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432498
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880842
ebirs730880842
HLIrs730880842
Exacrs730880842
Varsomers730880842
Maprs730880842
PheGenIrs730880842
hapmaprs730880842
1000 genomesrs730880842
hgdprs730880842
ensemblrs730880842
gopubmedrs730880842
geneviewrs730880842
scholarrs730880842
googlers730880842
pharmgkbrs730880842
gwascentralrs730880842
openSNPrs730880842
23andMers730880842
23andMe allrs730880842
SNP Nexus

SNPshotrs730880842
SNPdbers730880842
MSV3drs730880842
GWAS Ctlgrs730880842
Max Magnitude0
ClinVar
Risk rs730880842(C;C)
Alt rs730880842(C;C)
Reference rs730880842(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23901707T>G
CLNSRC
CLNACC RCV000158740.2,