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rs730880835

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880835(A;C)
Make rs730880835(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432704
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880835
ebirs730880835
HLIrs730880835
Exacrs730880835
Varsomers730880835
Maprs730880835
PheGenIrs730880835
hapmaprs730880835
1000 genomesrs730880835
hgdprs730880835
ensemblrs730880835
gopubmedrs730880835
geneviewrs730880835
scholarrs730880835
googlers730880835
pharmgkbrs730880835
gwascentralrs730880835
openSNPrs730880835
23andMers730880835
23andMe allrs730880835
SNP Nexus

SNPshotrs730880835
SNPdbers730880835
MSV3drs730880835
GWAS Ctlgrs730880835
Max Magnitude0
ClinVar
Risk rs730880835(C,T;C,T)
Alt rs730880835(C,T;C,T)
Reference rs730880835(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23901913T>A
CLNSRC
CLNACC RCV000168836.1,