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rs13097028

From SNPedia

Orientationplus
Stabilizedplus
Make rs13097028(C;C)
Make rs13097028(C;T)
Make rs13097028(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position169747154
is asnp
is mentioned by
dbSNPrs13097028
ebirs13097028
HLIrs13097028
Exacrs13097028
Varsomers13097028
Maprs13097028
PheGenIrs13097028
hapmaprs13097028
1000 genomesrs13097028
hgdprs13097028
ensemblrs13097028
gopubmedrs13097028
geneviewrs13097028
scholarrs13097028
googlers13097028
pharmgkbrs13097028
gwascentralrs13097028
openSNPrs13097028
23andMers13097028
23andMe allrs13097028
SNP Nexus

SNPshotrs13097028
SNPdbers13097028
MSV3drs13097028
GWAS Ctlgrs13097028
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24980573OA-icon.png]
Trait Melanoma
Title Identification of a melanoma susceptibility locus and somatic mutation in TET2.
Risk Allele
P-val 7E-7
Odds Ratio 1.12 [1.08-1.18]