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rs730880920

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880920(A;A)
Make rs730880920(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432647
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880920
ebirs730880920
HLIrs730880920
Exacrs730880920
Varsomers730880920
Maprs730880920
PheGenIrs730880920
hapmaprs730880920
1000 genomesrs730880920
hgdprs730880920
ensemblrs730880920
gopubmedrs730880920
geneviewrs730880920
scholarrs730880920
googlers730880920
pharmgkbrs730880920
gwascentralrs730880920
openSNPrs730880920
23andMers730880920
23andMe allrs730880920
SNP Nexus

SNPshotrs730880920
SNPdbers730880920
MSV3drs730880920
GWAS Ctlgrs730880920
Max Magnitude0
ClinVar
Risk rs730880920(A;A)
Alt rs730880920(A;A)
Reference rs730880920(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23901856A>T
CLNSRC
CLNACC RCV000158877.1,