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rs730880810

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880810(C;C)
Make rs730880810(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416129
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880810
ebirs730880810
HLIrs730880810
Exacrs730880810
Varsomers730880810
Maprs730880810
PheGenIrs730880810
hapmaprs730880810
1000 genomesrs730880810
hgdprs730880810
ensemblrs730880810
gopubmedrs730880810
geneviewrs730880810
scholarrs730880810
googlers730880810
pharmgkbrs730880810
gwascentralrs730880810
openSNPrs730880810
23andMers730880810
23andMe allrs730880810
SNP Nexus

SNPshotrs730880810
SNPdbers730880810
MSV3drs730880810
GWAS Ctlgrs730880810
Max Magnitude0
ClinVar
Risk rs730880810(C;C)
Alt rs730880810(C;C)
Reference rs730880810(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23885338C>G
CLNSRC
CLNACC RCV000158673.1,