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

rs2228607

From SNPedia

Orientationminus
Stabilizedminus
Make rs2228607(C;C)
Make rs2228607(C;T)
Make rs2228607(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position73708593
GeneSTX1A
is asnp
is mentioned by
dbSNPrs2228607
ebirs2228607
HLIrs2228607
Exacrs2228607
Varsomers2228607
Maprs2228607
PheGenIrs2228607
hapmaprs2228607
1000 genomesrs2228607
hgdprs2228607
ensemblrs2228607
gopubmedrs2228607
geneviewrs2228607
scholarrs2228607
googlers2228607
pharmgkbrs2228607
gwascentralrs2228607
openSNPrs2228607
23andMers2228607
23andMe allrs2228607
SNP Nexus

SNPshotrs2228607
SNPdbers2228607
MSV3drs2228607
GWAS Ctlgrs2228607
GMAF0.4894
Max Magnitude

[PMID 23572023OA-icon.png] Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A [PMID 18593506] Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism.