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rs730880869

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880869(A;T)
Make rs730880869(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429252
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880869
ebirs730880869
HLIrs730880869
Exacrs730880869
Varsomers730880869
Maprs730880869
PheGenIrs730880869
hapmaprs730880869
1000 genomesrs730880869
hgdprs730880869
ensemblrs730880869
gopubmedrs730880869
geneviewrs730880869
scholarrs730880869
googlers730880869
pharmgkbrs730880869
gwascentralrs730880869
openSNPrs730880869
23andMers730880869
23andMe allrs730880869
SNP Nexus

SNPshotrs730880869
SNPdbers730880869
MSV3drs730880869
GWAS Ctlgrs730880869
Max Magnitude0
ClinVar
Risk rs730880869(T;T)
Alt rs730880869(T;T)
Reference rs730880869(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23898461T>A
CLNSRC
CLNACC RCV000158791.2,