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rs730880822

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880822(A;A)
Make rs730880822(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415020
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880822
ebirs730880822
HLIrs730880822
Exacrs730880822
Varsomers730880822
Maprs730880822
PheGenIrs730880822
hapmaprs730880822
1000 genomesrs730880822
hgdprs730880822
ensemblrs730880822
gopubmedrs730880822
geneviewrs730880822
scholarrs730880822
googlers730880822
pharmgkbrs730880822
gwascentralrs730880822
openSNPrs730880822
23andMers730880822
23andMe allrs730880822
SNP Nexus

SNPshotrs730880822
SNPdbers730880822
MSV3drs730880822
GWAS Ctlgrs730880822
Max Magnitude0
ClinVar
Risk rs730880822(A;A)
Alt rs730880822(A;A)
Reference rs730880822(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23884229C>T
CLNSRC
CLNACC RCV000158707.2,