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rs1249277

From SNPedia

Orientationminus
Make rs1249277(C;C)
Make rs1249277(C;G)
Make rs1249277(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position28431147
is asnp
is mentioned by
dbSNPrs1249277
ebirs1249277
HLIrs1249277
Exacrs1249277
Varsomers1249277
Maprs1249277
PheGenIrs1249277
hapmaprs1249277
1000 genomesrs1249277
hgdprs1249277
ensemblrs1249277
gopubmedrs1249277
geneviewrs1249277
scholarrs1249277
googlers1249277
pharmgkbrs1249277
gwascentralrs1249277
openSNPrs1249277
23andMers1249277
23andMe allrs1249277
SNP Nexus

SNPshotrs1249277
SNPdbers1249277
MSV3drs1249277
GWAS Ctlgrs1249277
Max Magnitude

[PMID 25256078] Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study