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rs730880735

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880735(G;G)
Make rs730880735(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425417
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880735
ebirs730880735
HLIrs730880735
Exacrs730880735
Varsomers730880735
Maprs730880735
PheGenIrs730880735
hapmaprs730880735
1000 genomesrs730880735
hgdprs730880735
ensemblrs730880735
gopubmedrs730880735
geneviewrs730880735
scholarrs730880735
googlers730880735
pharmgkbrs730880735
gwascentralrs730880735
openSNPrs730880735
23andMers730880735
23andMe allrs730880735
SNP Nexus

SNPshotrs730880735
SNPdbers730880735
MSV3drs730880735
GWAS Ctlgrs730880735
Max Magnitude0
ClinVar
Risk rs730880735(G;G)
Alt rs730880735(G;G)
Reference rs730880735(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894626A>C
CLNSRC
CLNACC RCV000158525.1,