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rs467691

From SNPedia

Orientationplus
Stabilizedplus
Make rs467691(G;G)
Make rs467691(G;T)
Make rs467691(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position26914271
is asnp
is mentioned by
dbSNPrs467691
ebirs467691
HLIrs467691
Exacrs467691
Varsomers467691
Maprs467691
PheGenIrs467691
hapmaprs467691
1000 genomesrs467691
hgdprs467691
ensemblrs467691
gopubmedrs467691
geneviewrs467691
scholarrs467691
googlers467691
pharmgkbrs467691
gwascentralrs467691
openSNPrs467691
23andMers467691
23andMe allrs467691
SNP Nexus

SNPshotrs467691
SNPdbers467691
MSV3drs467691
GWAS Ctlgrs467691
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 23792102] Phenotype variations affect genetic association studies of degenerative disc disease: conclusions of analysis of genetic association of 58 single nucleotide polymorphisms with highly specific phenotypes for disc degeneration in 332 subjects