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rs1550976

From SNPedia

Orientationplus
Stabilizedplus
Make rs1550976(C;C)
Make rs1550976(C;T)
Make rs1550976(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position131450176
GeneNTM
is asnp
is mentioned by
dbSNPrs1550976
ebirs1550976
HLIrs1550976
Exacrs1550976
Varsomers1550976
Maprs1550976
PheGenIrs1550976
hapmaprs1550976
1000 genomesrs1550976
hgdprs1550976
ensemblrs1550976
gopubmedrs1550976
geneviewrs1550976
scholarrs1550976
googlers1550976
pharmgkbrs1550976
gwascentralrs1550976
openSNPrs1550976
23andMers1550976
23andMe allrs1550976
SNP Nexus

SNPshotrs1550976
SNPdbers1550976
MSV3drs1550976
GWAS Ctlgrs1550976
GMAF0.1823
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21182207OA-icon.png]
Trait
Title Variants in several genomic regions associated with Asperger disorder
Risk Allele
P-val 0.000003
Odds Ratio None None