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rs730880814

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880814(G;T)
Make rs730880814(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415401
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880814
ebirs730880814
HLIrs730880814
Exacrs730880814
Varsomers730880814
Maprs730880814
PheGenIrs730880814
hapmaprs730880814
1000 genomesrs730880814
hgdprs730880814
ensemblrs730880814
gopubmedrs730880814
geneviewrs730880814
scholarrs730880814
googlers730880814
pharmgkbrs730880814
gwascentralrs730880814
openSNPrs730880814
23andMers730880814
23andMe allrs730880814
SNP Nexus

SNPshotrs730880814
SNPdbers730880814
MSV3drs730880814
GWAS Ctlgrs730880814
Max Magnitude0
ClinVar
Risk rs730880814(T;T)
Alt rs730880814(T;T)
Reference rs730880814(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23884610C>A
CLNSRC
CLNACC RCV000158690.2,