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rs730880768

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880768(A;G)
Make rs730880768(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23422265
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880768
ebirs730880768
HLIrs730880768
Exacrs730880768
Varsomers730880768
Maprs730880768
PheGenIrs730880768
hapmaprs730880768
1000 genomesrs730880768
hgdprs730880768
ensemblrs730880768
gopubmedrs730880768
geneviewrs730880768
scholarrs730880768
googlers730880768
pharmgkbrs730880768
gwascentralrs730880768
openSNPrs730880768
23andMers730880768
23andMe allrs730880768
SNP Nexus

SNPshotrs730880768
SNPdbers730880768
MSV3drs730880768
GWAS Ctlgrs730880768
Max Magnitude0
ClinVar
Risk rs730880768(G;G)
Alt rs730880768(G;G)
Reference rs730880768(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23891474T>C
CLNSRC
CLNACC RCV000158591.1,