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rs730880769

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880769(A;A)
Make rs730880769(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23422262
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880769
ebirs730880769
HLIrs730880769
Exacrs730880769
Varsomers730880769
Maprs730880769
PheGenIrs730880769
hapmaprs730880769
1000 genomesrs730880769
hgdprs730880769
ensemblrs730880769
gopubmedrs730880769
geneviewrs730880769
scholarrs730880769
googlers730880769
pharmgkbrs730880769
gwascentralrs730880769
openSNPrs730880769
23andMers730880769
23andMe allrs730880769
SNP Nexus

SNPshotrs730880769
SNPdbers730880769
MSV3drs730880769
GWAS Ctlgrs730880769
Max Magnitude0
ClinVar
Risk rs730880769(A;A)
Alt rs730880769(A;A)
Reference rs730880769(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23891471G>T
CLNSRC
CLNACC RCV000158592.1,