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

rs892055

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs892055(A;G)
Make rs892055(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38422124
GeneRASGRP4
is asnp
is mentioned by
dbSNPrs892055
ebirs892055
HLIrs892055
Exacrs892055
Varsomers892055
Maprs892055
PheGenIrs892055
hapmaprs892055
1000 genomesrs892055
hgdprs892055
ensemblrs892055
gopubmedrs892055
geneviewrs892055
scholarrs892055
googlers892055
pharmgkbrs892055
gwascentralrs892055
openSNPrs892055
23andMers892055
23andMe allrs892055
SNP Nexus

SNPshotrs892055
SNPdbers892055
MSV3drs892055
GWAS Ctlgrs892055
GMAF0.4894
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21182207OA-icon.png]
Trait
Title Variants in several genomic regions associated with Asperger disorder
Risk Allele
P-val 0.000005
Odds Ratio None None


GET Evidence
RASGRP4-I18T
aa_change Ile18Thr
aa_change_short I18T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.422841
summary