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rs2127675

From SNPedia

Orientationminus
Stabilizedminus
Make rs2127675(C;C)
Make rs2127675(C;T)
Make rs2127675(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32883073
is asnp
is mentioned by
dbSNPrs2127675
ebirs2127675
HLIrs2127675
Exacrs2127675
Varsomers2127675
Maprs2127675
PheGenIrs2127675
hapmaprs2127675
1000 genomesrs2127675
hgdprs2127675
ensemblrs2127675
gopubmedrs2127675
geneviewrs2127675
scholarrs2127675
googlers2127675
pharmgkbrs2127675
gwascentralrs2127675
openSNPrs2127675
23andMers2127675
23andMe allrs2127675
SNP Nexus

SNPshotrs2127675
SNPdbers2127675
MSV3drs2127675
GWAS Ctlgrs2127675
GMAF0.3393
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23360169OA-icon.png] Association between putative functional variants in the PSMB9 gene and risk of melanoma - re-analysis of published melanoma genome-wide association studies