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rs730880836

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880836(A;C)
Make rs730880836(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432699
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880836
ebirs730880836
HLIrs730880836
Exacrs730880836
Varsomers730880836
Maprs730880836
PheGenIrs730880836
hapmaprs730880836
1000 genomesrs730880836
hgdprs730880836
ensemblrs730880836
gopubmedrs730880836
geneviewrs730880836
scholarrs730880836
googlers730880836
pharmgkbrs730880836
gwascentralrs730880836
openSNPrs730880836
23andMers730880836
23andMe allrs730880836
SNP Nexus

SNPshotrs730880836
SNPdbers730880836
MSV3drs730880836
GWAS Ctlgrs730880836
Max Magnitude0
ClinVar
Risk rs730880836(C,G;C,G)
Alt rs730880836(C,G;C,G)
Reference rs730880836(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23901908T>G
CLNSRC
CLNACC RCV000158734.1,