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rs730880863

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880863(C;C)
Make rs730880863(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429865
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880863
ebirs730880863
HLIrs730880863
Exacrs730880863
Varsomers730880863
Maprs730880863
PheGenIrs730880863
hapmaprs730880863
1000 genomesrs730880863
hgdprs730880863
ensemblrs730880863
gopubmedrs730880863
geneviewrs730880863
scholarrs730880863
googlers730880863
pharmgkbrs730880863
gwascentralrs730880863
openSNPrs730880863
23andMers730880863
23andMe allrs730880863
SNP Nexus

SNPshotrs730880863
SNPdbers730880863
MSV3drs730880863
GWAS Ctlgrs730880863
Max Magnitude0
ClinVar
Risk rs730880863(C;C)
Alt rs730880863(C;C)
Reference rs730880863(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23899074A>G
CLNSRC
CLNACC RCV000158780.2,