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rs730880820

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880820(A;A)
Make rs730880820(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415059
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880820
ebirs730880820
HLIrs730880820
Exacrs730880820
Varsomers730880820
Maprs730880820
PheGenIrs730880820
hapmaprs730880820
1000 genomesrs730880820
hgdprs730880820
ensemblrs730880820
gopubmedrs730880820
geneviewrs730880820
scholarrs730880820
googlers730880820
pharmgkbrs730880820
gwascentralrs730880820
openSNPrs730880820
23andMers730880820
23andMe allrs730880820
SNP Nexus

SNPshotrs730880820
SNPdbers730880820
MSV3drs730880820
GWAS Ctlgrs730880820
Max Magnitude0
ClinVar
Risk rs730880820(A;A)
Alt rs730880820(A;A)
Reference rs730880820(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23884268C>T
CLNSRC
CLNACC RCV000158704.3,