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rs730880757

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880757(C;C)
Make rs730880757(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424115
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880757
ebirs730880757
HLIrs730880757
Exacrs730880757
Varsomers730880757
Maprs730880757
PheGenIrs730880757
hapmaprs730880757
1000 genomesrs730880757
hgdprs730880757
ensemblrs730880757
gopubmedrs730880757
geneviewrs730880757
scholarrs730880757
googlers730880757
pharmgkbrs730880757
gwascentralrs730880757
openSNPrs730880757
23andMers730880757
23andMe allrs730880757
SNP Nexus

SNPshotrs730880757
SNPdbers730880757
MSV3drs730880757
GWAS Ctlgrs730880757
Max Magnitude0
ClinVar
Risk rs730880757(C;C)
Alt rs730880757(C;C)
Reference rs730880757(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893324C>G
CLNSRC
CLNACC RCV000158568.1,