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rs1811399

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G)
(T;T) 0
Make rs1811399(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position100862552
GeneNPAS2
is asnp
is mentioned by
dbSNPrs1811399
ebirs1811399
HLIrs1811399
Exacrs1811399
Varsomers1811399
Maprs1811399
PheGenIrs1811399
hapmaprs1811399
1000 genomesrs1811399
hgdprs1811399
ensemblrs1811399
gopubmedrs1811399
geneviewrs1811399
scholarrs1811399
googlers1811399
pharmgkbrs1811399
gwascentralrs1811399
openSNPrs1811399
23andMers1811399
23andMe allrs1811399
SNP Nexus

SNPshotrs1811399
SNPdbers1811399
MSV3drs1811399
GWAS Ctlgrs1811399
GMAF0.281
Max Magnitude0
? (G;G) (G;T) (T;T) 28
nature The inheritance of the AC haplotype of rs1861972rs1861973, the C allele of rs1811399, and the C allele of rs1234747 may contribute to autism by affecting microRNA


[PMID 17264841] Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis.


[PMID 20174623OA-icon.png] Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance.