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rs1859767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1859767(A;T)
Make rs1859767(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position108447879
GeneNRCAM
is asnp
is mentioned by
dbSNPrs1859767
ebirs1859767
HLIrs1859767
Exacrs1859767
Varsomers1859767
Maprs1859767
PheGenIrs1859767
hapmaprs1859767
1000 genomesrs1859767
hgdprs1859767
ensemblrs1859767
gopubmedrs1859767
geneviewrs1859767
scholarrs1859767
googlers1859767
pharmgkbrs1859767
gwascentralrs1859767
openSNPrs1859767
23andMers1859767
23andMe allrs1859767
SNP Nexus

SNPshotrs1859767
SNPdbers1859767
MSV3drs1859767
GWAS Ctlgrs1859767
GMAF0.3673
Max Magnitude0
? (A;A) (A;T) (T;T) 28

[PMID 18664314] Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism