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rs57244888

From SNPedia

Orientationplus
Stabilizedplus
Make rs57244888(C;C)
Make rs57244888(C;T)
Make rs57244888(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position16280877
is asnp
is mentioned by
dbSNPrs57244888
ebirs57244888
HLIrs57244888
Exacrs57244888
Varsomers57244888
Maprs57244888
PheGenIrs57244888
hapmaprs57244888
1000 genomesrs57244888
hgdprs57244888
ensemblrs57244888
gopubmedrs57244888
geneviewrs57244888
scholarrs57244888
googlers57244888
pharmgkbrs57244888
gwascentralrs57244888
openSNPrs57244888
23andMers57244888
23andMe allrs57244888
SNP Nexus

SNPshotrs57244888
SNPdbers57244888
MSV3drs57244888
GWAS Ctlgrs57244888
Max Magnitude

[PMID 25855136OA-icon.png] New basal cell carcinoma susceptibility loci