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rs28934598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs28934598(C;T)
Make rs28934598(T;T)
ReferenceGRCh37.p2 37.2/134
Chromosome4
Position57461227
GeneLOC100506564
is asnp
is mentioned by
dbSNPrs28934598
ebirs28934598
HLIrs28934598
Exacrs28934598
Varsomers28934598
Maprs28934598
PheGenIrs28934598
hapmaprs28934598
1000 genomesrs28934598
hgdprs28934598
ensemblrs28934598
gopubmedrs28934598
geneviewrs28934598
scholarrs28934598
googlers28934598
pharmgkbrs28934598
gwascentralrs28934598
openSNPrs28934598
23andMers28934598
23andMe allrs28934598
SNP Nexus

SNPshotrs28934598
SNPdbers28934598
MSV3drs28934598
GWAS Ctlgrs28934598
StatusDeleted
Max Magnitude0
OMIM238300
DescGLYCINE ENCEPHALOPATHY
Variant0006
Relatedalso