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rs730880807

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880807(A;A)
Make rs730880807(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416248
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880807
ebirs730880807
HLIrs730880807
Exacrs730880807
Varsomers730880807
Maprs730880807
PheGenIrs730880807
hapmaprs730880807
1000 genomesrs730880807
hgdprs730880807
ensemblrs730880807
gopubmedrs730880807
geneviewrs730880807
scholarrs730880807
googlers730880807
pharmgkbrs730880807
gwascentralrs730880807
openSNPrs730880807
23andMers730880807
23andMe allrs730880807
SNP Nexus

SNPshotrs730880807
SNPdbers730880807
MSV3drs730880807
GWAS Ctlgrs730880807
Max Magnitude0
ClinVar
Risk rs730880807(A;A)
Alt rs730880807(A;A)
Reference rs730880807(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23885457G>T
CLNSRC
CLNACC RCV000158668.2,