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

rs730880944

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880944(C;C)
Make rs730880944(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position110919144
GeneMYL2
is asnp
is mentioned by
dbSNPrs730880944
ebirs730880944
HLIrs730880944
Exacrs730880944
Varsomers730880944
Maprs730880944
PheGenIrs730880944
hapmaprs730880944
1000 genomesrs730880944
hgdprs730880944
ensemblrs730880944
gopubmedrs730880944
geneviewrs730880944
scholarrs730880944
googlers730880944
pharmgkbrs730880944
gwascentralrs730880944
openSNPrs730880944
23andMers730880944
23andMe allrs730880944
SNP Nexus

SNPshotrs730880944
SNPdbers730880944
MSV3drs730880944
GWAS Ctlgrs730880944
Max Magnitude0
ClinVar
Risk rs730880944(C;C)
Alt rs730880944(C;C)
Reference rs730880944(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYL2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.111356948A>G
CLNSRC
CLNACC RCV000158913.2,