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rs730880915

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880915(C;T)
Make rs730880915(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415721
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880915
ebirs730880915
HLIrs730880915
Exacrs730880915
Varsomers730880915
Maprs730880915
PheGenIrs730880915
hapmaprs730880915
1000 genomesrs730880915
hgdprs730880915
ensemblrs730880915
gopubmedrs730880915
geneviewrs730880915
scholarrs730880915
googlers730880915
pharmgkbrs730880915
gwascentralrs730880915
openSNPrs730880915
23andMers730880915
23andMe allrs730880915
SNP Nexus

SNPshotrs730880915
SNPdbers730880915
MSV3drs730880915
GWAS Ctlgrs730880915
Max Magnitude0
ClinVar
Risk rs730880915(G,T;G,T)
Alt rs730880915(G,T;G,T)
Reference rs730880915(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23884930G>A
CLNSRC
CLNACC RCV000158870.2,