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rs9891263

From SNPedia

Orientationplus
Stabilizedplus
Make rs9891263(C;C)
Make rs9891263(C;T)
Make rs9891263(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position54859747
is asnp
is mentioned by
dbSNPrs9891263
ebirs9891263
HLIrs9891263
Exacrs9891263
Varsomers9891263
Maprs9891263
PheGenIrs9891263
hapmaprs9891263
1000 genomesrs9891263
hgdprs9891263
ensemblrs9891263
gopubmedrs9891263
geneviewrs9891263
scholarrs9891263
googlers9891263
pharmgkbrs9891263
gwascentralrs9891263
openSNPrs9891263
23andMers9891263
23andMe allrs9891263
SNP Nexus

SNPshotrs9891263
SNPdbers9891263
MSV3drs9891263
GWAS Ctlgrs9891263
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25227856] Exploratory investigation of genetic associations with Basal cell carcinoma risk: genome-wide association study in jeju island, Korea