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rs11959298

From SNPedia

Orientationplus
Stabilizedplus
Make rs11959298(A;A)
Make rs11959298(A;G)
Make rs11959298(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position135031850
GeneLOC100996485, PITX1
is asnp
is mentioned by
dbSNPrs11959298
ebirs11959298
HLIrs11959298
Exacrs11959298
Varsomers11959298
Maprs11959298
PheGenIrs11959298
hapmaprs11959298
1000 genomesrs11959298
hgdprs11959298
ensemblrs11959298
gopubmedrs11959298
geneviewrs11959298
scholarrs11959298
googlers11959298
pharmgkbrs11959298
gwascentralrs11959298
openSNPrs11959298
23andMers11959298
23andMe allrs11959298
SNP Nexus

SNPshotrs11959298
SNPdbers11959298
MSV3drs11959298
GWAS Ctlgrs11959298
GMAF0.202
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 18053270OA-icon.png] Individuals homozygous or heterozygous for the rs11959298(A)-rs6596189(C) haplotype risk allele were 2.54 and 1.59 fold more likely to have autism, respectively, compared to rs11959298(G)-rs6596189(T) carriers.

Note/caveat emptor: ~90% of the world's population carries what the authors from this for-profit genetic testing company call the "risk haplotype", yet the frequency of autism is less than 1% (perhaps 1 in 150).

Neighborrs6596189
Distance629