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rs730880902

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880902(A;A)
Make rs730880902(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23423687
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880902
ebirs730880902
HLIrs730880902
Exacrs730880902
Varsomers730880902
Maprs730880902
PheGenIrs730880902
hapmaprs730880902
1000 genomesrs730880902
hgdprs730880902
ensemblrs730880902
gopubmedrs730880902
geneviewrs730880902
scholarrs730880902
googlers730880902
pharmgkbrs730880902
gwascentralrs730880902
openSNPrs730880902
23andMers730880902
23andMe allrs730880902
SNP Nexus

SNPshotrs730880902
SNPdbers730880902
MSV3drs730880902
GWAS Ctlgrs730880902
Max Magnitude0
ClinVar
Risk rs730880902(A;A)
Alt rs730880902(A;A)
Reference rs730880902(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23892896C>T
CLNSRC
CLNACC RCV000158856.2,