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rs730880947

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880947(A;G)
Make rs730880947(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position110915771
GeneMYL2
is asnp
is mentioned by
dbSNPrs730880947
ebirs730880947
HLIrs730880947
Exacrs730880947
Varsomers730880947
Maprs730880947
PheGenIrs730880947
hapmaprs730880947
1000 genomesrs730880947
hgdprs730880947
ensemblrs730880947
gopubmedrs730880947
geneviewrs730880947
scholarrs730880947
googlers730880947
pharmgkbrs730880947
gwascentralrs730880947
openSNPrs730880947
23andMers730880947
23andMe allrs730880947
SNP Nexus

SNPshotrs730880947
SNPdbers730880947
MSV3drs730880947
GWAS Ctlgrs730880947
Max Magnitude0
ClinVar
Risk rs730880947(G;G)
Alt rs730880947(G;G)
Reference rs730880947(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYL2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.111353575T>C
CLNSRC
CLNACC RCV000158918.2,