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rs730880821

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880821(A;A)
Make rs730880821(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415024
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880821
ebirs730880821
HLIrs730880821
Exacrs730880821
Varsomers730880821
Maprs730880821
PheGenIrs730880821
hapmaprs730880821
1000 genomesrs730880821
hgdprs730880821
ensemblrs730880821
gopubmedrs730880821
geneviewrs730880821
scholarrs730880821
googlers730880821
pharmgkbrs730880821
gwascentralrs730880821
openSNPrs730880821
23andMers730880821
23andMe allrs730880821
SNP Nexus

SNPshotrs730880821
SNPdbers730880821
MSV3drs730880821
GWAS Ctlgrs730880821
Max Magnitude0
ClinVar
Risk rs730880821(A;A)
Alt rs730880821(A;A)
Reference rs730880821(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23884233C>T
CLNSRC
CLNACC RCV000158706.2,