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rs730880815

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880815(A;A)
Make rs730880815(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415237
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880815
ebirs730880815
HLIrs730880815
Exacrs730880815
Varsomers730880815
Maprs730880815
PheGenIrs730880815
hapmaprs730880815
1000 genomesrs730880815
hgdprs730880815
ensemblrs730880815
gopubmedrs730880815
geneviewrs730880815
scholarrs730880815
googlers730880815
pharmgkbrs730880815
gwascentralrs730880815
openSNPrs730880815
23andMers730880815
23andMe allrs730880815
SNP Nexus

SNPshotrs730880815
SNPdbers730880815
MSV3drs730880815
GWAS Ctlgrs730880815
Max Magnitude0
ClinVar
Risk rs730880815(A;A)
Alt rs730880815(A;A)
Reference rs730880815(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23884446G>T
CLNSRC
CLNACC RCV000158693.3,