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rs730880899

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880899(C;C)
Make rs730880899(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424904
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880899
ebirs730880899
HLIrs730880899
Exacrs730880899
Varsomers730880899
Maprs730880899
PheGenIrs730880899
hapmaprs730880899
1000 genomesrs730880899
hgdprs730880899
ensemblrs730880899
gopubmedrs730880899
geneviewrs730880899
scholarrs730880899
googlers730880899
pharmgkbrs730880899
gwascentralrs730880899
openSNPrs730880899
23andMers730880899
23andMe allrs730880899
SNP Nexus

SNPshotrs730880899
SNPdbers730880899
MSV3drs730880899
GWAS Ctlgrs730880899
Max Magnitude0
ClinVar
Risk rs730880899(C;C)
Alt rs730880899(C;C)
Reference rs730880899(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23894113C>G
CLNSRC
CLNACC RCV000221330.1,