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rs2209852

From SNPedia

Orientationplus
Stabilizedplus
Make rs2209852(A;A)
Make rs2209852(A;G)
Make rs2209852(G;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position94865368
GeneLOC101927284
is asnp
is mentioned by
dbSNPrs2209852
ebirs2209852
HLIrs2209852
Exacrs2209852
Varsomers2209852
Maprs2209852
PheGenIrs2209852
hapmaprs2209852
1000 genomesrs2209852
hgdprs2209852
ensemblrs2209852
gopubmedrs2209852
geneviewrs2209852
scholarrs2209852
googlers2209852
pharmgkbrs2209852
gwascentralrs2209852
openSNPrs2209852
23andMers2209852
23andMe allrs2209852
SNP Nexus

SNPshotrs2209852
SNPdbers2209852
MSV3drs2209852
GWAS Ctlgrs2209852
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24571439OA-icon.png]
Trait Parent of origin effect on language impairment (paternal)
Title Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
Risk Allele
P-val 6E-6
Odds Ratio NR NR