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rs730880870

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880870(A;A)
Make rs730880870(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429037
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880870
ebirs730880870
HLIrs730880870
Exacrs730880870
Varsomers730880870
Maprs730880870
PheGenIrs730880870
hapmaprs730880870
1000 genomesrs730880870
hgdprs730880870
ensemblrs730880870
gopubmedrs730880870
geneviewrs730880870
scholarrs730880870
googlers730880870
pharmgkbrs730880870
gwascentralrs730880870
openSNPrs730880870
23andMers730880870
23andMe allrs730880870
SNP Nexus

SNPshotrs730880870
SNPdbers730880870
MSV3drs730880870
GWAS Ctlgrs730880870
Max Magnitude0
ClinVar
Risk rs730880870(A;A)
Alt rs730880870(A;A)
Reference rs730880870(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23898246C>T
CLNSRC
CLNACC RCV000158796.2,