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rs2073559

From SNPedia

Orientationplus
Stabilizedplus
Make rs2073559(C;C)
Make rs2073559(C;T)
Make rs2073559(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position103678477
GeneRELN
is asnp
is mentioned by
dbSNPrs2073559
ebirs2073559
HLIrs2073559
Exacrs2073559
Varsomers2073559
Maprs2073559
PheGenIrs2073559
hapmaprs2073559
1000 genomesrs2073559
hgdprs2073559
ensemblrs2073559
gopubmedrs2073559
geneviewrs2073559
scholarrs2073559
googlers2073559
pharmgkbrs2073559
gwascentralrs2073559
openSNPrs2073559
23andMers2073559
23andMe allrs2073559
SNP Nexus

SNPshotrs2073559
SNPdbers2073559
MSV3drs2073559
GWAS Ctlgrs2073559
GMAF0.472
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20554015] No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population


[PMID 17621165] Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.