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rs11055880

From SNPedia

Orientationplus
Stabilizedplus
Make rs11055880(C;C)
Make rs11055880(C;T)
Make rs11055880(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position14257700
is asnp
is mentioned by
dbSNPrs11055880
dbSNP (old)rs11055880
ClinGenrs11055880
ebirs11055880
HLIrs11055880
Exacrs11055880
Gnomadrs11055880
Varsomers11055880
LitVarrs11055880
Maprs11055880
PheGenIrs11055880
Biobankrs11055880
1000 genomesrs11055880
hgdprs11055880
ensemblrs11055880
gopubmedrs11055880
geneviewrs11055880
scholarrs11055880
googlers11055880
pharmgkbrs11055880
gwascentralrs11055880
openSNPrs11055880
23andMers11055880
23andMe allrs11055880
SNPshotrs11055880
SNPdbers11055880
MSV3drs11055880
GWAS Ctlgrs11055880
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 29061142OA-icon.png] Systematic identification of regulatory variants associated with cancer risk.