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rs730880925

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880925(C;C)
Make rs730880925(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429309
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880925
ebirs730880925
HLIrs730880925
Exacrs730880925
Varsomers730880925
Maprs730880925
PheGenIrs730880925
hapmaprs730880925
1000 genomesrs730880925
hgdprs730880925
ensemblrs730880925
gopubmedrs730880925
geneviewrs730880925
scholarrs730880925
googlers730880925
pharmgkbrs730880925
gwascentralrs730880925
openSNPrs730880925
23andMers730880925
23andMe allrs730880925
SNP Nexus

SNPshotrs730880925
SNPdbers730880925
MSV3drs730880925
GWAS Ctlgrs730880925
Max Magnitude0
ClinVar
Risk rs730880925(C;C)
Alt rs730880925(C;C)
Reference rs730880925(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23898518C>G
CLNSRC
CLNACC RCV000158884.2,