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rs730880747

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880747(A;A)
Make rs730880747(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424930
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880747
ebirs730880747
HLIrs730880747
Exacrs730880747
Varsomers730880747
Maprs730880747
PheGenIrs730880747
hapmaprs730880747
1000 genomesrs730880747
hgdprs730880747
ensemblrs730880747
gopubmedrs730880747
geneviewrs730880747
scholarrs730880747
googlers730880747
pharmgkbrs730880747
gwascentralrs730880747
openSNPrs730880747
23andMers730880747
23andMe allrs730880747
SNP Nexus

SNPshotrs730880747
SNPdbers730880747
MSV3drs730880747
GWAS Ctlgrs730880747
Max Magnitude0
ClinVar
Risk rs730880747(A;A)
Alt rs730880747(A;A)
Reference rs730880747(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894139G>T
CLNSRC
CLNACC RCV000158544.2,