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rs6617

From SNPedia

Orientationplus
Stabilizedplus
Make rs6617(C;C)
Make rs6617(C;G)
Make rs6617(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome3
Position52706166
GeneGLT8D1, SPCS1
is asnp
is mentioned by
dbSNPrs6617
dbSNP (classic)rs6617
ClinGenrs6617
ebirs6617
HLIrs6617
Exacrs6617
Gnomadrs6617
Varsomers6617
LitVarrs6617
Maprs6617
PheGenIrs6617
Biobankrs6617
1000 genomesrs6617
hgdprs6617
ensemblrs6617
geneviewrs6617
scholarrs6617
googlers6617
pharmgkbrs6617
gwascentralrs6617
openSNPrs6617
23andMers6617
SNPshotrs6617
SNPdbers6617
MSV3drs6617
GWAS Ctlgrs6617
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 29942097OA-icon.png] Common variants in the GNL3 contribute to the increasing risk of knee osteoarthritis in Han Chinese population.