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rs1557765

From SNPedia

Orientationminus
Stabilizedminus
Make rs1557765(A;A)
Make rs1557765(A;G)
Make rs1557765(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position17382092
is asnp
is mentioned by
dbSNPrs1557765
ebirs1557765
HLIrs1557765
Exacrs1557765
Varsomers1557765
Maprs1557765
PheGenIrs1557765
hapmaprs1557765
1000 genomesrs1557765
hgdprs1557765
ensemblrs1557765
gopubmedrs1557765
geneviewrs1557765
scholarrs1557765
googlers1557765
pharmgkbrs1557765
gwascentralrs1557765
openSNPrs1557765
23andMers1557765
23andMe allrs1557765
SNP Nexus

SNPshotrs1557765
SNPdbers1557765
MSV3drs1557765
GWAS Ctlgrs1557765
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24564958OA-icon.png]
Trait Social communication problems
Title Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence.
Risk Allele C
P-val 7E-6
Odds Ratio .12 [0.061-0.179] unit increase