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rs730880950

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880950(C;C)
Make rs730880950(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position110914203
GeneMYL2
is asnp
is mentioned by
dbSNPrs730880950
ebirs730880950
HLIrs730880950
Exacrs730880950
Varsomers730880950
Maprs730880950
PheGenIrs730880950
hapmaprs730880950
1000 genomesrs730880950
hgdprs730880950
ensemblrs730880950
gopubmedrs730880950
geneviewrs730880950
scholarrs730880950
googlers730880950
pharmgkbrs730880950
gwascentralrs730880950
openSNPrs730880950
23andMers730880950
23andMe allrs730880950
SNP Nexus

SNPshotrs730880950
SNPdbers730880950
MSV3drs730880950
GWAS Ctlgrs730880950
Max Magnitude0
ClinVar
Risk rs730880950(C;C)
Alt rs730880950(C;C)
Reference rs730880950(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYL2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.111352007A>G
CLNSRC
CLNACC RCV000158925.1,