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rs730880804

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880804(A;C)
Make rs730880804(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416869
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880804
ebirs730880804
HLIrs730880804
Exacrs730880804
Varsomers730880804
Maprs730880804
PheGenIrs730880804
hapmaprs730880804
1000 genomesrs730880804
hgdprs730880804
ensemblrs730880804
gopubmedrs730880804
geneviewrs730880804
scholarrs730880804
googlers730880804
pharmgkbrs730880804
gwascentralrs730880804
openSNPrs730880804
23andMers730880804
23andMe allrs730880804
SNP Nexus

SNPshotrs730880804
SNPdbers730880804
MSV3drs730880804
GWAS Ctlgrs730880804
Max Magnitude0
ClinVar
Risk rs730880804(C;C)
Alt rs730880804(C;C)
Reference rs730880804(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23886078T>G
CLNSRC
CLNACC RCV000158664.1,