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rs736707

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs736707(C;C)
Make rs736707(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position103489956
GeneLOC101927870, RELN
is asnp
is mentioned by
dbSNPrs736707
ebirs736707
HLIrs736707
Exacrs736707
Varsomers736707
Maprs736707
PheGenIrs736707
hapmaprs736707
1000 genomesrs736707
hgdprs736707
ensemblrs736707
gopubmedrs736707
geneviewrs736707
scholarrs736707
googlers736707
pharmgkbrs736707
gwascentralrs736707
openSNPrs736707
23andMers736707
23andMe allrs736707
SNP Nexus

SNPshotrs736707
SNPdbers736707
MSV3drs736707
GWAS Ctlgrs736707
GMAF0.3407
Max Magnitude0
? (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 18597938] Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.


[PMID 23216241OA-icon.png] Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.