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rs730880817

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880817(C;T)
Make rs730880817(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415155
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880817
ebirs730880817
HLIrs730880817
Exacrs730880817
Varsomers730880817
Maprs730880817
PheGenIrs730880817
hapmaprs730880817
1000 genomesrs730880817
hgdprs730880817
ensemblrs730880817
gopubmedrs730880817
geneviewrs730880817
scholarrs730880817
googlers730880817
pharmgkbrs730880817
gwascentralrs730880817
openSNPrs730880817
23andMers730880817
23andMe allrs730880817
SNP Nexus

SNPshotrs730880817
SNPdbers730880817
MSV3drs730880817
GWAS Ctlgrs730880817
Max Magnitude0
ClinVar
Risk rs730880817(T;T)
Alt rs730880817(T;T)
Reference rs730880817(C;C)
Significance Other
Disease not provided not specified
Variation info
Gene MYH7 MHRT
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23884364G>A
CLNSRC
CLNACC RCV000158699.2, RCV000214438.1,