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rs730880864

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880864(A;G)
Make rs730880864(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429862
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880864
ebirs730880864
HLIrs730880864
Exacrs730880864
Varsomers730880864
Maprs730880864
PheGenIrs730880864
hapmaprs730880864
1000 genomesrs730880864
hgdprs730880864
ensemblrs730880864
gopubmedrs730880864
geneviewrs730880864
scholarrs730880864
googlers730880864
pharmgkbrs730880864
gwascentralrs730880864
openSNPrs730880864
23andMers730880864
23andMe allrs730880864
SNP Nexus

SNPshotrs730880864
SNPdbers730880864
MSV3drs730880864
GWAS Ctlgrs730880864
Max Magnitude0
ClinVar
Risk rs730880864(G;G)
Alt rs730880864(G;G)
Reference rs730880864(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23899071T>C
CLNSRC
CLNACC RCV000158781.2,