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rs730880734

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880734(G;T)
Make rs730880734(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425818
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880734
ebirs730880734
HLIrs730880734
Exacrs730880734
Varsomers730880734
Maprs730880734
PheGenIrs730880734
hapmaprs730880734
1000 genomesrs730880734
hgdprs730880734
ensemblrs730880734
gopubmedrs730880734
geneviewrs730880734
scholarrs730880734
googlers730880734
pharmgkbrs730880734
gwascentralrs730880734
openSNPrs730880734
23andMers730880734
23andMe allrs730880734
SNP Nexus

SNPshotrs730880734
SNPdbers730880734
MSV3drs730880734
GWAS Ctlgrs730880734
Max Magnitude0
ClinVar
Risk rs730880734(T;T)
Alt rs730880734(T;T)
Reference rs730880734(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23895027C>A
CLNSRC
CLNACC RCV000158515.1,