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rs730880880

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880880(A;G)
Make rs730880880(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23427668
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880880
ebirs730880880
HLIrs730880880
Exacrs730880880
Varsomers730880880
Maprs730880880
PheGenIrs730880880
hapmaprs730880880
1000 genomesrs730880880
hgdprs730880880
ensemblrs730880880
gopubmedrs730880880
geneviewrs730880880
scholarrs730880880
googlers730880880
pharmgkbrs730880880
gwascentralrs730880880
openSNPrs730880880
23andMers730880880
23andMe allrs730880880
SNP Nexus

SNPshotrs730880880
SNPdbers730880880
MSV3drs730880880
GWAS Ctlgrs730880880
Max Magnitude0
ClinVar
Risk rs730880880(G;G)
Alt rs730880880(G;G)
Reference rs730880880(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23896877T>C
CLNSRC
CLNACC RCV000158817.1,