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rs730880760

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880760(A;G)
Make rs730880760(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424037
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880760
ebirs730880760
HLIrs730880760
Exacrs730880760
Varsomers730880760
Maprs730880760
PheGenIrs730880760
hapmaprs730880760
1000 genomesrs730880760
hgdprs730880760
ensemblrs730880760
gopubmedrs730880760
geneviewrs730880760
scholarrs730880760
googlers730880760
pharmgkbrs730880760
gwascentralrs730880760
openSNPrs730880760
23andMers730880760
23andMe allrs730880760
SNP Nexus

SNPshotrs730880760
SNPdbers730880760
MSV3drs730880760
GWAS Ctlgrs730880760
Max Magnitude0
ClinVar
Risk rs730880760(G;G)
Alt rs730880760(G;G)
Reference rs730880760(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893246T>C
CLNSRC
CLNACC RCV000158576.1,