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rs730880843

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880843(A;C)
Make rs730880843(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431850
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880843
ebirs730880843
HLIrs730880843
Exacrs730880843
Varsomers730880843
Maprs730880843
PheGenIrs730880843
hapmaprs730880843
1000 genomesrs730880843
hgdprs730880843
ensemblrs730880843
gopubmedrs730880843
geneviewrs730880843
scholarrs730880843
googlers730880843
pharmgkbrs730880843
gwascentralrs730880843
openSNPrs730880843
23andMers730880843
23andMe allrs730880843
SNP Nexus

SNPshotrs730880843
SNPdbers730880843
MSV3drs730880843
GWAS Ctlgrs730880843
Max Magnitude0
ClinVar
Risk rs730880843(C;C)
Alt rs730880843(C;C)
Reference rs730880843(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23901059T>G
CLNSRC
CLNACC RCV000158743.2,