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rs2293507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2293507(G;T)
Make rs2293507(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position70763034
GeneAUTS2
is asnp
is mentioned by
dbSNPrs2293507
ebirs2293507
HLIrs2293507
Exacrs2293507
Varsomers2293507
Maprs2293507
PheGenIrs2293507
hapmaprs2293507
1000 genomesrs2293507
hgdprs2293507
ensemblrs2293507
gopubmedrs2293507
geneviewrs2293507
scholarrs2293507
googlers2293507
pharmgkbrs2293507
gwascentralrs2293507
openSNPrs2293507
23andMers2293507
23andMe allrs2293507
SNP Nexus

SNPshotrs2293507
SNPdbers2293507
MSV3drs2293507
GWAS Ctlgrs2293507
GMAF0.07117
Max Magnitude0
? (G;G) (G;T) (T;T) 28
Venter snp
Source plos
Gene AUTS2
allele T
frequency 0.033
sift TOLERATED
HuRef 1103652606825
Disease Association This gene is interrupted by a translocation breakpoint in a pair of autistic twins.



GET Evidence
AUTS2-A303S
aa_change Ala303Ser
aa_change_short A303S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0799405
summary