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rs28937585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs28937585(G;G)
Make rs28937585(G;T)
ReferenceGRCh37 37.1/131
Chromosome12
Position52294822
is asnp
is mentioned by
dbSNPrs28937585
ebirs28937585
HLIrs28937585
Exacrs28937585
Varsomers28937585
Maprs28937585
PheGenIrs28937585
hapmaprs28937585
1000 genomesrs28937585
hgdprs28937585
ensemblrs28937585
gopubmedrs28937585
geneviewrs28937585
scholarrs28937585
googlers28937585
pharmgkbrs28937585
gwascentralrs28937585
openSNPrs28937585
23andMers28937585
23andMe allrs28937585
SNP Nexus

SNPshotrs28937585
SNPdbers28937585
MSV3drs28937585
GWAS Ctlgrs28937585
StatusDeleted
Max Magnitude0
OMIM603381
DescLARSEN SYNDROME, AUTOSOMAL DOMINANT
Variant0004
Relatedalso
Neighborrs28937586
Distance36