Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880898

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880898(A;A)
Make rs730880898(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424970
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880898
ebirs730880898
HLIrs730880898
Exacrs730880898
Varsomers730880898
Maprs730880898
PheGenIrs730880898
hapmaprs730880898
1000 genomesrs730880898
hgdprs730880898
ensemblrs730880898
gopubmedrs730880898
geneviewrs730880898
scholarrs730880898
googlers730880898
pharmgkbrs730880898
gwascentralrs730880898
openSNPrs730880898
23andMers730880898
23andMe allrs730880898
SNP Nexus

SNPshotrs730880898
SNPdbers730880898
MSV3drs730880898
GWAS Ctlgrs730880898
Max Magnitude0
ClinVar
Risk rs730880898(A;A)
Alt rs730880898(A;A)
Reference rs730880898(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894179A>T
CLNSRC
CLNACC RCV000158844.1,