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rs730880948

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880948(G;T)
Make rs730880948(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position110920526
GeneMYL2
is asnp
is mentioned by
dbSNPrs730880948
ebirs730880948
HLIrs730880948
Exacrs730880948
Varsomers730880948
Maprs730880948
PheGenIrs730880948
hapmaprs730880948
1000 genomesrs730880948
hgdprs730880948
ensemblrs730880948
gopubmedrs730880948
geneviewrs730880948
scholarrs730880948
googlers730880948
pharmgkbrs730880948
gwascentralrs730880948
openSNPrs730880948
23andMers730880948
23andMe allrs730880948
SNP Nexus

SNPshotrs730880948
SNPdbers730880948
MSV3drs730880948
GWAS Ctlgrs730880948
Max Magnitude0
ClinVar
Risk rs730880948(T;T)
Alt rs730880948(T;T)
Reference rs730880948(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYL2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.111358330C>A
CLNSRC
CLNACC RCV000158921.2,