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rs2229864

From SNPedia

Orientationminus
Stabilizedminus
Make rs2229864(C;C)
Make rs2229864(C;T)
Make rs2229864(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position103515258
GeneRELN
is asnp
is mentioned by
dbSNPrs2229864
ClinGenrs2229864
ebirs2229864
HLIrs2229864
Exacrs2229864
Varsomers2229864
Maprs2229864
PheGenIrs2229864
hapmaprs2229864
1000 genomesrs2229864
hgdprs2229864
ensemblrs2229864
gopubmedrs2229864
geneviewrs2229864
scholarrs2229864
googlers2229864
pharmgkbrs2229864
gwascentralrs2229864
openSNPrs2229864
23andMers2229864
23andMe allrs2229864
SNP Nexus

SNPshotrs2229864
SNPdbers2229864
MSV3drs2229864
GWAS Ctlgrs2229864
GMAF0.4256
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


ClinVar
Risk rs2229864(C;C)
Alt rs2229864(C;C)
Reference rs2229864(T;T)
Significance Other
Disease not specified Lissencephaly
Variation info
Gene RELN
CLNDBN not specified Lissencephaly, Recessive
Reversed 1
HGVS NC_000007.13:g.103155705A>G
CLNSRC ClinVar Emory University University of Chicago
CLNACC RCV000081242.8, RCV000404542.1,