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rs730880878

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880878(A;A)
Make rs730880878(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23427792
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880878
ebirs730880878
HLIrs730880878
Exacrs730880878
Varsomers730880878
Maprs730880878
PheGenIrs730880878
hapmaprs730880878
1000 genomesrs730880878
hgdprs730880878
ensemblrs730880878
gopubmedrs730880878
geneviewrs730880878
scholarrs730880878
googlers730880878
pharmgkbrs730880878
gwascentralrs730880878
openSNPrs730880878
23andMers730880878
23andMe allrs730880878
SNP Nexus

SNPshotrs730880878
SNPdbers730880878
MSV3drs730880878
GWAS Ctlgrs730880878
Max Magnitude0
ClinVar
Risk rs730880878(A,T;A,T)
Alt rs730880878(A,T;A,T)
Reference rs730880878(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23897001C>T
CLNSRC
CLNACC RCV000158812.2,