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SNP Report
Name | rs2885470 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:197748569 - 197748569(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.263379 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000273582, ENST00000428738, ENST00000467303, ENST00000472149); non_coding_transcript_variant(ENST00000467303, ENST00000472149); upstream_gene_variant(ENST00000241502, ENST00000412924, ENST00000415708, ENST00000418169, ENST00000424384, ENST00000426031, ENST00000494309) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
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.