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rs1411771

From SNPedia

Orientationplus
Stabilizedplus
Make rs1411771(C;C)
Make rs1411771(C;T)
Make rs1411771(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position232039029
GeneDISC1, MAP1LC3C
is asnp
is mentioned by
dbSNPrs1411771
ebirs1411771
HLIrs1411771
Exacrs1411771
Varsomers1411771
Maprs1411771
PheGenIrs1411771
hapmaprs1411771
1000 genomesrs1411771
hgdprs1411771
ensemblrs1411771
gopubmedrs1411771
geneviewrs1411771
scholarrs1411771
googlers1411771
pharmgkbrs1411771
gwascentralrs1411771
openSNPrs1411771
23andMers1411771
23andMe allrs1411771
SNP Nexus

SNPshotrs1411771
SNPdbers1411771
MSV3drs1411771
GWAS Ctlgrs1411771
GMAF0.3517
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 17673452] 13 single-nucleotide polymorphisms (SNPs) in 723 members of 179 Finnish Bipolar disorder families.
  • rs751229(T) and rs3738401(A) was over-transmitted to males with psychotic disorder.
  • under-transmitted rs821616(T) and rs1411771(T)
  • The risk haplotype for psychotic disorder also associated to perseverations (P = 0.035; for rs751229 alone P = 0.0012), and a protective haplotype G-T-G with rs1655285 in addition to auditory attention (P = 0.0059).


[PMID 20084519] Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging