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rs730880868

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880868(A;A)
Make rs730880868(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429255
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880868
ebirs730880868
HLIrs730880868
Exacrs730880868
Varsomers730880868
Maprs730880868
PheGenIrs730880868
hapmaprs730880868
1000 genomesrs730880868
hgdprs730880868
ensemblrs730880868
gopubmedrs730880868
geneviewrs730880868
scholarrs730880868
googlers730880868
pharmgkbrs730880868
gwascentralrs730880868
openSNPrs730880868
23andMers730880868
23andMe allrs730880868
SNP Nexus

SNPshotrs730880868
SNPdbers730880868
MSV3drs730880868
GWAS Ctlgrs730880868
Max Magnitude0
ClinVar
Risk rs730880868(A;A)
Alt rs730880868(A;A)
Reference rs730880868(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23898464C>T
CLNSRC
CLNACC RCV000158790.2,