Have questions? Visit https://www.reddit.com/r/SNPedia

rs1896731

From SNPedia

Orientationplus
Stabilizedplus
Make rs1896731(C;C)
Make rs1896731(C;T)
Make rs1896731(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position25898911
is asnp
is mentioned by
dbSNPrs1896731
ebirs1896731
HLIrs1896731
Exacrs1896731
Varsomers1896731
Maprs1896731
PheGenIrs1896731
hapmaprs1896731
1000 genomesrs1896731
hgdprs1896731
ensemblrs1896731
gopubmedrs1896731
geneviewrs1896731
scholarrs1896731
googlers1896731
pharmgkbrs1896731
gwascentralrs1896731
openSNPrs1896731
23andMers1896731
23andMe allrs1896731
SNP Nexus

SNPshotrs1896731
SNPdbers1896731
MSV3drs1896731
GWAS Ctlgrs1896731
GMAF0.4449
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19456320OA-icon.png] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.


GET Evidence
rs1896731
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.4375
summary