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rs730880772

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880772(C;C)
Make rs730880772(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23421025
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880772
ebirs730880772
HLIrs730880772
Exacrs730880772
Varsomers730880772
Maprs730880772
PheGenIrs730880772
hapmaprs730880772
1000 genomesrs730880772
hgdprs730880772
ensemblrs730880772
gopubmedrs730880772
geneviewrs730880772
scholarrs730880772
googlers730880772
pharmgkbrs730880772
gwascentralrs730880772
openSNPrs730880772
23andMers730880772
23andMe allrs730880772
SNP Nexus

SNPshotrs730880772
SNPdbers730880772
MSV3drs730880772
GWAS Ctlgrs730880772
Max Magnitude0
ClinVar
Risk rs730880772(C;C)
Alt rs730880772(C;C)
Reference rs730880772(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23890234A>G
CLNSRC
CLNACC RCV000158599.2,