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rs730880846

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880846(A;G)
Make rs730880846(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431783
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880846
ebirs730880846
HLIrs730880846
Exacrs730880846
Varsomers730880846
Maprs730880846
PheGenIrs730880846
hapmaprs730880846
1000 genomesrs730880846
hgdprs730880846
ensemblrs730880846
gopubmedrs730880846
geneviewrs730880846
scholarrs730880846
googlers730880846
pharmgkbrs730880846
gwascentralrs730880846
openSNPrs730880846
23andMers730880846
23andMe allrs730880846
SNP Nexus

SNPshotrs730880846
SNPdbers730880846
MSV3drs730880846
GWAS Ctlgrs730880846
Max Magnitude0
ClinVar
Risk rs730880846(G;G)
Alt rs730880846(G;G)
Reference rs730880846(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23900992T>C
CLNSRC
CLNACC RCV000158751.2,