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rs17042407

From SNPedia

Orientationplus
Stabilizedplus
Make rs17042407(C;C)
Make rs17042407(C;T)
Make rs17042407(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position112801337
is asnp
is mentioned by
dbSNPrs17042407
ebirs17042407
HLIrs17042407
Exacrs17042407
Varsomers17042407
Maprs17042407
PheGenIrs17042407
hapmaprs17042407
1000 genomesrs17042407
hgdprs17042407
ensemblrs17042407
gopubmedrs17042407
geneviewrs17042407
scholarrs17042407
googlers17042407
pharmgkbrs17042407
gwascentralrs17042407
openSNPrs17042407
23andMers17042407
23andMe allrs17042407
SNP Nexus

SNPshotrs17042407
SNPdbers17042407
MSV3drs17042407
GWAS Ctlgrs17042407
GMAF0.2011
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 24615437] Genetic variants in the IL1A gene region contribute to intestinal-type gastric carcinoma susceptibility in European populations [PMID 19626699OA-icon.png] Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations.