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rs730880847

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880847(C;C)
Make rs730880847(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431668
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880847
ebirs730880847
HLIrs730880847
Exacrs730880847
Varsomers730880847
Maprs730880847
PheGenIrs730880847
hapmaprs730880847
1000 genomesrs730880847
hgdprs730880847
ensemblrs730880847
gopubmedrs730880847
geneviewrs730880847
scholarrs730880847
googlers730880847
pharmgkbrs730880847
gwascentralrs730880847
openSNPrs730880847
23andMers730880847
23andMe allrs730880847
SNP Nexus

SNPshotrs730880847
SNPdbers730880847
MSV3drs730880847
GWAS Ctlgrs730880847
Max Magnitude0
ClinVar
Risk rs730880847(C;C)
Alt rs730880847(C;C)
Reference rs730880847(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23900877C>G
CLNSRC
CLNACC RCV000158754.1,