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rs1049346

From SNPedia

Orientationminus
Make rs1049346(C;C)
Make rs1049346(C;T)
Make rs1049346(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position38703061
GeneGLO1
is asnp
is mentioned by
dbSNPrs1049346
ebirs1049346
HLIrs1049346
Exacrs1049346
Varsomers1049346
Maprs1049346
PheGenIrs1049346
hapmaprs1049346
1000 genomesrs1049346
hgdprs1049346
ensemblrs1049346
gopubmedrs1049346
geneviewrs1049346
scholarrs1049346
googlers1049346
pharmgkbrs1049346
gwascentralrs1049346
openSNPrs1049346
23andMers1049346
23andMe allrs1049346
SNP Nexus

SNPshotrs1049346
SNPdbers1049346
MSV3drs1049346
GWAS Ctlgrs1049346
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25201284] The GLO1 C332 (Ala111) allele confers autism vulnerability: family-based genetic association and functional correlates


[PMID 27000251] Role of glyoxalase I gene polymorphisms in late-onset epilepsy and drug-resistant epilepsy The CC genotype of rs1049346 protects against late-onset epilepsy and drug resistant epilepsy. The presence of the TAC/AAT haplotypes (rs1130534-rs4746-rs1049346) may be used as a marker of predisposition to/protection against drug resistant epilepsy. rs1049346 is not on the typically used gene chips, though there is a perfect proxy, Rs1781735, on the 23andme v3 chip. Risk by genotype will be posted to the rs1781735 page.