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rs28934579

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
(T;T) 0 common in complete genomics
Make rs28934579(C;C)
Make rs28934579(C;T)
ReferenceGRCh37 37.1/131
Chromosome11
Position2189379
GeneTH
is asnp
is mentioned by
dbSNPrs28934579
ClinGenrs28934579
ebirs28934579
HLIrs28934579
Exacrs28934579
Varsomers28934579
Maprs28934579
PheGenIrs28934579
hapmaprs28934579
1000 genomesrs28934579
hgdprs28934579
ensemblrs28934579
gopubmedrs28934579
geneviewrs28934579
scholarrs28934579
googlers28934579
pharmgkbrs28934579
gwascentralrs28934579
openSNPrs28934579
23andMers28934579
23andMe allrs28934579
SNP Nexus

SNPshotrs28934579
SNPdbers28934579
MSV3drs28934579
GWAS Ctlgrs28934579
StatusDeleted
Max Magnitude0
OMIM191290
DescSEGAWA SYNDROME, AUTOSOMAL RECESSIVE
Variant0002
Relatedalso