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rs730880867

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880867(A;A)
Make rs730880867(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429276
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880867
ebirs730880867
HLIrs730880867
Exacrs730880867
Varsomers730880867
Maprs730880867
PheGenIrs730880867
hapmaprs730880867
1000 genomesrs730880867
hgdprs730880867
ensemblrs730880867
gopubmedrs730880867
geneviewrs730880867
scholarrs730880867
googlers730880867
pharmgkbrs730880867
gwascentralrs730880867
openSNPrs730880867
23andMers730880867
23andMe allrs730880867
SNP Nexus

SNPshotrs730880867
SNPdbers730880867
MSV3drs730880867
GWAS Ctlgrs730880867
Max Magnitude0
ClinVar
Risk rs730880867(A;A)
Alt rs730880867(A;A)
Reference rs730880867(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23898485C>T
CLNSRC
CLNACC RCV000158789.1,