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rs730880952

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880952(G;T)
Make rs730880952(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position110911082
GeneMYL2
is asnp
is mentioned by
dbSNPrs730880952
ebirs730880952
HLIrs730880952
Exacrs730880952
Varsomers730880952
Maprs730880952
PheGenIrs730880952
hapmaprs730880952
1000 genomesrs730880952
hgdprs730880952
ensemblrs730880952
gopubmedrs730880952
geneviewrs730880952
scholarrs730880952
googlers730880952
pharmgkbrs730880952
gwascentralrs730880952
openSNPrs730880952
23andMers730880952
23andMe allrs730880952
SNP Nexus

SNPshotrs730880952
SNPdbers730880952
MSV3drs730880952
GWAS Ctlgrs730880952
Max Magnitude0
ClinVar
Risk rs730880952(T;T)
Alt rs730880952(T;T)
Reference rs730880952(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYL2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.111348886C>A
CLNSRC
CLNACC RCV000158935.2,