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SNP Report
Name | rs10995315 dbSNP Ensembl | ||
---|---|---|---|
Location | chr10:62814811 - 62814811(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.0894569 | ||
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 | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | YES | ||
Overlap with MDD? | NO |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.
Reference | Statistical Result | Description | Result Category |
---|---|---|---|
Kim, S. H.,2011 | For SZ, chi-square tests:allele, OR=1.116, X2=0.3138, P-value = 0.5754, P-value(permutation)=0.99;Fisher's exact test, genotype, X2=2.8926, P-value = 0.2354 | No significant association was observed. | Negative |