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SNP Report
Name | rs885861 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:159028856 - 159028856(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.310104 | ||
Functional Annotation | 3_prime_UTR_variant; downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000262178); downstream_gene_variant(ENST00000377633, ENST00000402066, ENST00000438049); non_coding_transcript_exon_variant(ENST00000413238); non_coding_transcript_variant(ENST00000413238) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | YES |
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 |
---|---|---|---|
Soria, V.,2010 | X2-tests:allele P-value = 0.009, Model Recessive, genotype P-value = 0.004, OR(95%CI)=1.71 (1.18-2.46) | Significant association was found. | Positive |