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rs17651822

From SNPedia

Orientationplus
Stabilizedplus
Make rs17651822(C;C)
Make rs17651822(C;T)
Make rs17651822(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position28678635
GeneLINC00693
is asnp
is mentioned by
dbSNPrs17651822
dbSNP (classic)rs17651822
ClinGenrs17651822
ebirs17651822
HLIrs17651822
Exacrs17651822
Gnomadrs17651822
Varsomers17651822
LitVarrs17651822
Maprs17651822
PheGenIrs17651822
Biobankrs17651822
1000 genomesrs17651822
hgdprs17651822
ensemblrs17651822
geneviewrs17651822
scholarrs17651822
googlers17651822
pharmgkbrs17651822
gwascentralrs17651822
openSNPrs17651822
23andMers17651822
SNPshotrs17651822
SNPdbers17651822
MSV3drs17651822
GWAS Ctlgrs17651822
GMAF0.09917
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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[PMID 17357082OA-icon.png] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.