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rs730880816

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880816(A;A)
Make rs730880816(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415159
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880816
ebirs730880816
HLIrs730880816
Exacrs730880816
Varsomers730880816
Maprs730880816
PheGenIrs730880816
hapmaprs730880816
1000 genomesrs730880816
hgdprs730880816
ensemblrs730880816
gopubmedrs730880816
geneviewrs730880816
scholarrs730880816
googlers730880816
pharmgkbrs730880816
gwascentralrs730880816
openSNPrs730880816
23andMers730880816
23andMe allrs730880816
SNP Nexus

SNPshotrs730880816
SNPdbers730880816
MSV3drs730880816
GWAS Ctlgrs730880816
Max Magnitude0
ClinVar
Risk rs730880816(A;A)
Alt rs730880816(A;A)
Reference rs730880816(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23884368C>T
CLNSRC
CLNACC RCV000158698.1,