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rs17780102

From SNPedia

Orientationplus
Stabilizedplus
Make rs17780102(A;A)
Make rs17780102(A;G)
Make rs17780102(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position3599443
is asnp
is mentioned by
dbSNPrs17780102
ebirs17780102
HLIrs17780102
Exacrs17780102
Varsomers17780102
Maprs17780102
PheGenIrs17780102
hapmaprs17780102
1000 genomesrs17780102
hgdprs17780102
ensemblrs17780102
gopubmedrs17780102
geneviewrs17780102
scholarrs17780102
googlers17780102
pharmgkbrs17780102
gwascentralrs17780102
openSNPrs17780102
23andMers17780102
23andMe allrs17780102
SNP Nexus

SNPshotrs17780102
SNPdbers17780102
MSV3drs17780102
GWAS Ctlgrs17780102
GMAF0.3779
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22688887OA-icon.png] Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma