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rs730880839

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880839(A;G)
Make rs730880839(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432648
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880839
ebirs730880839
HLIrs730880839
Exacrs730880839
Varsomers730880839
Maprs730880839
PheGenIrs730880839
hapmaprs730880839
1000 genomesrs730880839
hgdprs730880839
ensemblrs730880839
gopubmedrs730880839
geneviewrs730880839
scholarrs730880839
googlers730880839
pharmgkbrs730880839
gwascentralrs730880839
openSNPrs730880839
23andMers730880839
23andMe allrs730880839
SNP Nexus

SNPshotrs730880839
SNPdbers730880839
MSV3drs730880839
GWAS Ctlgrs730880839
Max Magnitude0
ClinVar
Risk rs730880839(G;G)
Alt rs730880839(G;G)
Reference rs730880839(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYH7
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23901857T>C
CLNSRC
CLNACC RCV000158737.2, RCV000223786.1,