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rs16849083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16849083(C;T)
Make rs16849083(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position139465437
GeneRBP2, RP11-319G6.1
is asnp
is mentioned by
dbSNPrs16849083
ebirs16849083
HLIrs16849083
Exacrs16849083
Varsomers16849083
Maprs16849083
PheGenIrs16849083
hapmaprs16849083
1000 genomesrs16849083
hgdprs16849083
ensemblrs16849083
gopubmedrs16849083
geneviewrs16849083
scholarrs16849083
googlers16849083
pharmgkbrs16849083
gwascentralrs16849083
openSNPrs16849083
23andMers16849083
23andMe allrs16849083
SNP Nexus

SNPshotrs16849083
SNPdbers16849083
MSV3drs16849083
GWAS Ctlgrs16849083
GMAF0.1097
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 21326860OA-icon.png] Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study