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rs2050656

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2050656(A;A)
Make rs2050656(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position237347614
GeneRYR2
is asnp
is mentioned by
dbSNPrs2050656
ebirs2050656
HLIrs2050656
Exacrs2050656
Varsomers2050656
Maprs2050656
PheGenIrs2050656
hapmaprs2050656
1000 genomesrs2050656
hgdprs2050656
ensemblrs2050656
gopubmedrs2050656
geneviewrs2050656
scholarrs2050656
googlers2050656
pharmgkbrs2050656
gwascentralrs2050656
openSNPrs2050656
23andMers2050656
23andMe allrs2050656
SNP Nexus

SNPshotrs2050656
SNPdbers2050656
MSV3drs2050656
GWAS Ctlgrs2050656
GMAF0.1837
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.[PMID 19626040OA-icon.png]