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rs730880849

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880849(C;C)
Make rs730880849(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431587
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880849
ebirs730880849
HLIrs730880849
Exacrs730880849
Varsomers730880849
Maprs730880849
PheGenIrs730880849
hapmaprs730880849
1000 genomesrs730880849
hgdprs730880849
ensemblrs730880849
gopubmedrs730880849
geneviewrs730880849
scholarrs730880849
googlers730880849
pharmgkbrs730880849
gwascentralrs730880849
openSNPrs730880849
23andMers730880849
23andMe allrs730880849
SNP Nexus

SNPshotrs730880849
SNPdbers730880849
MSV3drs730880849
GWAS Ctlgrs730880849
Max Magnitude0
ClinVar
Risk rs730880849(C;C)
Alt rs730880849(C;C)
Reference rs730880849(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23900796A>G
CLNSRC
CLNACC RCV000158757.2,