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rs10038113

From SNPedia

Orientationplus
Stabilizedplus
Make rs10038113(C;C)
Make rs10038113(C;T)
Make rs10038113(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position25902233
is asnp
is mentioned by
dbSNPrs10038113
ebirs10038113
HLIrs10038113
Exacrs10038113
Varsomers10038113
Maprs10038113
PheGenIrs10038113
hapmaprs10038113
1000 genomesrs10038113
hgdprs10038113
ensemblrs10038113
gopubmedrs10038113
geneviewrs10038113
scholarrs10038113
googlers10038113
pharmgkbrs10038113
gwascentralrs10038113
openSNPrs10038113
23andMers10038113
23andMe allrs10038113
SNP Nexus

SNPshotrs10038113
SNPdbers10038113
MSV3drs10038113
GWAS Ctlgrs10038113
GMAF0.4885
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19456320OA-icon.png]
Trait Autism
Title A genome-wide association study of autism reveals a common novel risk locus at 5p14.1
Risk Allele T
P-val 0.000003
Odds Ratio 1.33 [1.11-1.43]


OMIM209850
Desc
Variant
Relatedalso
OMIM209850
Desc
Variant
Relatedalso


GET Evidence
rs10038113
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484127
summary