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rs730880763

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880763(C;C)
Make rs730880763(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23423626
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880763
ebirs730880763
HLIrs730880763
Exacrs730880763
Varsomers730880763
Maprs730880763
PheGenIrs730880763
hapmaprs730880763
1000 genomesrs730880763
hgdprs730880763
ensemblrs730880763
gopubmedrs730880763
geneviewrs730880763
scholarrs730880763
googlers730880763
pharmgkbrs730880763
gwascentralrs730880763
openSNPrs730880763
23andMers730880763
23andMe allrs730880763
SNP Nexus

SNPshotrs730880763
SNPdbers730880763
MSV3drs730880763
GWAS Ctlgrs730880763
Max Magnitude0
ClinVar
Risk rs730880763(C;C)
Alt rs730880763(C;C)
Reference rs730880763(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23892835A>G
CLNSRC
CLNACC RCV000158583.1,