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rs2229860

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2229860(C;G)
Make rs2229860(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position103565380
GeneRELN
is asnp
is mentioned by
dbSNPrs2229860
ebirs2229860
HLIrs2229860
Exacrs2229860
Varsomers2229860
Maprs2229860
PheGenIrs2229860
hapmaprs2229860
1000 genomesrs2229860
hgdprs2229860
ensemblrs2229860
gopubmedrs2229860
geneviewrs2229860
scholarrs2229860
googlers2229860
pharmgkbrs2229860
gwascentralrs2229860
openSNPrs2229860
23andMers2229860
23andMe allrs2229860
SNP Nexus

SNPshotrs2229860
SNPdbers2229860
MSV3drs2229860
GWAS Ctlgrs2229860
Max Magnitude0
? (C;C) (C;G) (G;G) 28

[PMID 19435634] Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia


ClinVar
Risk rs2229860(G;G)
Alt rs2229860(G;G)
Reference rs2229860(C;C)
Significance Other
Disease not specified
Variation info
Gene RELN
CLNDBN not specified
Reversed 1
HGVS NC_000007.13:g.103205827G>C
CLNSRC ClinVar University of Chicago
CLNACC RCV000118154.3,