Search SNP
Search Gene
Search CNV
Search Haplotype
Search Other Variant
Search Region
Search Pathway
Search Study
SNP Report
Name | rs2297488 dbSNP Ensembl | ||
---|---|---|---|
Location | chr10:62815485 - 62815485(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.0892572 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000242480, ENST00000411732, ENST00000439032, ENST00000493899, ENST00000637191, LRG_239t1); non_coding_transcript_variant(ENST00000493899) | ||
No. of Studies | 3 (Positive: 1; Negative: 2; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | YES | ||
Overlap with MDD? | NO |
Reference | Statistical Result | Description | Result Category |
---|---|---|---|
Kim, S. H.,2011 | For SZ, chi-square tests:allele, OR=1.114, X2=0.3127, P-value = 0.576, P-value(permutation)=0.5592;Fisher's exact test, genotype, X2=2.9107, P-value = 0.2333 | No significant association was observed. | Negative |