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rs8766

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs8766(A;G)
Make rs8766(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position55228300
GeneTCF4
is asnp
is mentioned by
dbSNPrs8766
ebirs8766
HLIrs8766
Exacrs8766
Varsomers8766
Maprs8766
PheGenIrs8766
hapmaprs8766
1000 genomesrs8766
hgdprs8766
ensemblrs8766
gopubmedrs8766
geneviewrs8766
scholarrs8766
googlers8766
pharmgkbrs8766
gwascentralrs8766
openSNPrs8766
23andMers8766
23andMe allrs8766
SNP Nexus

SNPshotrs8766
SNPdbers8766
MSV3drs8766
GWAS Ctlgrs8766
Max Magnitude0

[PMID 27305091] Genetic Association of TCF4 and AKT1 Gene Variants with the Age at Onset of Schizophrenia.

ClinVar
Risk rs8766(G;G)
Alt rs8766(G;G)
Reference rs8766(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene TCF4
CLNDBN not specified
Reversed 1
HGVS NC_000018.9:g.52895531T>C
CLNSRC
CLNACC RCV000079460.6,