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rs833497

From SNPedia

Orientationplus
Stabilizedplus
Make rs833497(C;C)
Make rs833497(C;T)
Make rs833497(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position49081890
GeneDYM
is asnp
is mentioned by
dbSNPrs833497
ebirs833497
HLIrs833497
Exacrs833497
Varsomers833497
Maprs833497
PheGenIrs833497
hapmaprs833497
1000 genomesrs833497
hgdprs833497
ensemblrs833497
gopubmedrs833497
geneviewrs833497
scholarrs833497
googlers833497
pharmgkbrs833497
gwascentralrs833497
openSNPrs833497
23andMers833497
23andMe allrs833497
SNP Nexus

SNPshotrs833497
SNPdbers833497
MSV3drs833497
GWAS Ctlgrs833497
GMAF0.2066
Max Magnitude
? (C;C) (C;T) (T;T) 28

A recent study in a Japanese population found that each C allele at rs833497 in the DYM gene is associated with 1.16x higher odds of schizophrenia. [PMID 20555340]

Defects in the DYM gene are also associated with Dyggve-Melchior-Clausen syndrome, an extremely rare disease found mostly among families with Lebanese or Spanish ancestry. [PMID 679519] [PMID 17288936]