Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880765

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880765(A;A)
Make rs730880765(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23423552
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880765
ebirs730880765
HLIrs730880765
Exacrs730880765
Varsomers730880765
Maprs730880765
PheGenIrs730880765
hapmaprs730880765
1000 genomesrs730880765
hgdprs730880765
ensemblrs730880765
gopubmedrs730880765
geneviewrs730880765
scholarrs730880765
googlers730880765
pharmgkbrs730880765
gwascentralrs730880765
openSNPrs730880765
23andMers730880765
23andMe allrs730880765
SNP Nexus

SNPshotrs730880765
SNPdbers730880765
MSV3drs730880765
GWAS Ctlgrs730880765
Max Magnitude0
ClinVar
Risk rs730880765(A;A)
Alt rs730880765(A;A)
Reference rs730880765(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23892761C>T
CLNSRC
CLNACC RCV000158585.2,