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rs730880848

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880848(G;T)
Make rs730880848(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431620
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880848
ebirs730880848
HLIrs730880848
Exacrs730880848
Varsomers730880848
Maprs730880848
PheGenIrs730880848
hapmaprs730880848
1000 genomesrs730880848
hgdprs730880848
ensemblrs730880848
gopubmedrs730880848
geneviewrs730880848
scholarrs730880848
googlers730880848
pharmgkbrs730880848
gwascentralrs730880848
openSNPrs730880848
23andMers730880848
23andMe allrs730880848
SNP Nexus

SNPshotrs730880848
SNPdbers730880848
MSV3drs730880848
GWAS Ctlgrs730880848
Max Magnitude0
ClinVar
Risk rs730880848(T;T)
Alt rs730880848(T;T)
Reference rs730880848(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23900829C>A
CLNSRC
CLNACC RCV000158755.2,